DMD Rabbit Polyclonal Antibody
DMD Rabbit Polyclonal Antibody
![]() Mouse Dystrophin (DMD) ELISA Kit |
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DLR-DMD-Mu-96T | DL Develop | 96T | 793.2 EUR |
Description: A sandwich quantitative ELISA assay kit for detection of Mouse Dystrophin (DMD) in samples from tissue homogenates, cell lysates or other biological fluids. |
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![]() Human Dystrophin (DMD) ELISA Kit |
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RD-DMD-Hu-48Tests | Reddot Biotech | 48 Tests | 600 EUR |
![]() Human Dystrophin (DMD) ELISA Kit |
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RD-DMD-Hu-96Tests | Reddot Biotech | 96 Tests | 830.4 EUR |
![]() Mouse Dystrophin (DMD) ELISA Kit |
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RD-DMD-Mu-48Tests | Reddot Biotech | 48 Tests | 613.2 EUR |
![]() Mouse Dystrophin (DMD) ELISA Kit |
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RD-DMD-Mu-96Tests | Reddot Biotech | 96 Tests | 850.8 EUR |
![]() Human Dystrophin (DMD) ELISA Kit |
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RDR-DMD-Hu-48Tests | Reddot Biotech | 48 Tests | 626.4 EUR |
![]() Human Dystrophin (DMD) ELISA Kit |
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RDR-DMD-Hu-96Tests | Reddot Biotech | 96 Tests | 868.8 EUR |
![]() Mouse Dystrophin (DMD) ELISA Kit |
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RDR-DMD-Mu-48Tests | Reddot Biotech | 48 Tests | 640.8 EUR |
![]() Mouse Dystrophin (DMD) ELISA Kit |
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RDR-DMD-Mu-96Tests | Reddot Biotech | 96 Tests | 890.4 EUR |
![]() DMD Polyclonal Antibody |
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ES9017-100ul | ELK Biotech | 100ul | 334.8 EUR |
Description: A Rabbit Polyclonal antibody against DMD from Human/Mouse/Rat. This antibody is tested and validated for IHC |
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![]() DMD Polyclonal Antibody |
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ES9017-50ul | ELK Biotech | 50ul | 248.4 EUR |
Description: A Rabbit Polyclonal antibody against DMD from Human/Mouse/Rat. This antibody is tested and validated for IHC |
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![]() DMD Polyclonal Antibody |
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ABP58391-003ml | Abbkine | 0.03ml | 189.6 EUR |
Description: A polyclonal antibody for detection of DMD from Human, Mouse, Rat. This DMD antibody is for IHC-P. It is affinity-purified from rabbit serum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from part region of human DMD protein |
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![]() DMD Polyclonal Antibody |
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ABP58391-01ml | Abbkine | 0.1ml | 346.8 EUR |
Description: A polyclonal antibody for detection of DMD from Human, Mouse, Rat. This DMD antibody is for IHC-P. It is affinity-purified from rabbit serum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from part region of human DMD protein |
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![]() DMD Polyclonal Antibody |
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ABP58391-02ml | Abbkine | 0.2ml | 496.8 EUR |
Description: A polyclonal antibody for detection of DMD from Human, Mouse, Rat. This DMD antibody is for IHC-P. It is affinity-purified from rabbit serum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from part region of human DMD protein |
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![]() DMD Rabbit pAb |
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A1411-100ul | Abclonal | 100 ul | 369.6 EUR |
![]() DMD Rabbit pAb |
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A1411-200ul | Abclonal | 200 ul | 550.8 EUR |
![]() DMD Rabbit pAb |
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A1411-20ul | Abclonal | 20 ul | 219.6 EUR |
![]() DMD Rabbit pAb |
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A1411-50ul | Abclonal | 50 ul | 267.6 EUR |
![]() Polyclonal DMD / Dystrophin Antibody |
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APR11762G | Leading Biology | 0.05mg | 580.8 EUR |
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human DMD / Dystrophin . This antibody is tested and proven to work in the following applications: |
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![]() Rabbit DMD ELISA Kit |
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ERTD0036 | Abclonal | 96Tests | 625.2 EUR |
![]() DMD Antibody |
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1-CSB-PA503789 | Cusabio |
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Description: A polyclonal antibody against DMD. Recognizes DMD from Human, Mouse. This antibody is Unconjugated. Tested in the following application: ELISA, IHC;ELISA:1:1000-1:2000, IHC:1:25-1:100 |
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![]() DMD Antibody |
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1-CSB-PA006963GA01HU | Cusabio |
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Description: A polyclonal antibody against DMD. Recognizes DMD from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB |
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![]() DMD Antibody |
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1-CSB-PA006963LA01HU | Cusabio |
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Description: A polyclonal antibody against DMD. Recognizes DMD from Human. This antibody is Unconjugated. Tested in the following application: ELISA, IHC; Recommended dilution: IHC:1:200-1:500 |
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![]() DMD antibody |
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70R-16862 | Fitzgerald | 50 ul | 522 EUR |
Description: Rabbit polyclonal DMD antibody |
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![]() DMD Antibody |
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36428-100ul | SAB | 100ul | 302.4 EUR |
![]() Dystrophin (DMD) Polyclonal Antibody (Human) |
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4-PAB503Hu01 | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD) |
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![]() Dystrophin (DMD) Polyclonal Antibody (Mouse) |
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4-PAB503Mu01 | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD) |
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![]() Rabbit Dystrophin (DMD) ELISA Kit |
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abx355333-96tests | Abbexa | 96 tests | 990 EUR |
![]() DMD Conjugated Antibody |
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C36428 | SAB | 100ul | 476.4 EUR |
![]() anti- DMD antibody |
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FNab02423 | FN Test | 100µg | 606.3 EUR |
Description: Antibody raised against DMD |
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![]() Dystrophin (DMD) Antibody |
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20-abx100315 | Abbexa |
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![]() Dystrophin (DMD) Antibody |
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20-abx100316 | Abbexa |
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![]() Dystrophin (DMD) Antibody |
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20-abx172180 | Abbexa |
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![]() Dystrophin (DMD) Antibody |
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20-abx149852 | Abbexa |
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![]() Dystrophin (DMD) Antibody |
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20-abx112214 | Abbexa |
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![]() Dystrophin (DMD) Antibody |
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20-abx001224 | Abbexa |
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![]() Dystrophin (DMD) Antibody |
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20-abx211560 | Abbexa |
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![]() Dystrophin (DMD) Antibody |
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abx232423-100ug | Abbexa | 100 ug | 577.2 EUR |
![]() Dystrophin (DMD) Antibody |
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20-abx176215 | Abbexa |
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![]() Anti-DMD antibody |
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PAab02423 | Lifescience Market | 100 ug | 426 EUR |
![]() Anti-DMD antibody |
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STJ23394 | St John's Laboratory | 100 µl | 332.4 EUR |
Description: This gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. |
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![]() Anti-DMD antibody |
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STJ190175 | St John's Laboratory | 200 µl | 236.4 EUR |
Description: Unconjugated Rabbit polyclonal to DMD |
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![]() Dystrophin Antibody / DMD |
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RQ5369 | NSJ Bioreagents | 100 ul | 419 EUR |
![]() Dystrophin Antibody / DMD |
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V8443-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V8443-20UG | NSJ Bioreagents | 20 ug | 219 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V8443SAF-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7540-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7540-20UG | NSJ Bioreagents | 20 ug | 219 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7540IHC-7ML | NSJ Bioreagents | 7 ml | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7540SAF-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7547-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7547-20UG | NSJ Bioreagents | 20 ug | 219 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7547IHC-7ML | NSJ Bioreagents | 7 ml | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7547SAF-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7548-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7548-20UG | NSJ Bioreagents | 20 ug | 219 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7548IHC-7ML | NSJ Bioreagents | 7 ml | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7548SAF-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7555-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq] |
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![]() Dystrophin Antibody / DMD |
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V7555-20UG | NSJ Bioreagents | 20 ug | 219 EUR |
Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq] |
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![]() Dystrophin Antibody / DMD |
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V7555IHC-7ML | NSJ Bioreagents | 7 ml | 499 EUR |
Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq] |
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![]() Dystrophin Antibody / DMD |
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V7555SAF-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq] |
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![]() Dystrophin Antibody / DMD |
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V7561-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7561-20UG | NSJ Bioreagents | 20 ug | 219 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7561IHC-7ML | NSJ Bioreagents | 7 ml | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7561SAF-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7562-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7562-20UG | NSJ Bioreagents | 20 ug | 219 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7562IHC-7ML | NSJ Bioreagents | 7 ml | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V7562SAF-100UG | NSJ Bioreagents | 100 ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V8862-100UG | NSJ Bioreagents | 100ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V8862-20UG | NSJ Bioreagents | 20ug | 219 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V8862SAF-100UG | NSJ Bioreagents | 100ug | 499 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V4009-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V4009-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin Antibody / DMD |
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V4009SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Human), APC |
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4-PAB503Hu01-APC | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with APC. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Human), Biotinylated |
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4-PAB503Hu01-Biotin | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with Biotin. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Human), Cy3 |
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4-PAB503Hu01-Cy3 | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with Cy3. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Human), FITC |
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4-PAB503Hu01-FITC | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with FITC. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Human), HRP |
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4-PAB503Hu01-HRP | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with HRP. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Human), PE |
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4-PAB503Hu01-PE | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with PE. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Mouse), APC |
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4-PAB503Mu01-APC | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with APC. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Mouse), Biotinylated |
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4-PAB503Mu01-Biotin | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with Biotin. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Mouse), Cy3 |
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4-PAB503Mu01-Cy3 | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with Cy3. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Mouse), FITC |
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4-PAB503Mu01-FITC | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with FITC. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Mouse), HRP |
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4-PAB503Mu01-HRP | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with HRP. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Mouse), PE |
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4-PAB503Mu01-PE | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with PE. |
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![]() DMD siRNA |
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20-abx914266 | Abbexa |
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![]() DMD siRNA |
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20-abx914267 | Abbexa |
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![]() Dystrophin (DMD) Polyclonal Antibody (Human), APC-Cy7 |
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4-PAB503Hu01-APC-Cy7 | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with APC-Cy7. |
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![]() Dystrophin (DMD) Polyclonal Antibody (Mouse), APC-Cy7 |
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4-PAB503Mu01-APC-Cy7 | Cloud-Clone |
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Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with APC-Cy7. |
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![]() DMD Antibody, HRP conjugated |
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1-CSB-PA006963LB01HU | Cusabio |
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Description: A polyclonal antibody against DMD. Recognizes DMD from Human. This antibody is HRP conjugated. Tested in the following application: ELISA |
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![]() DMD Antibody, FITC conjugated |
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1-CSB-PA006963LC01HU | Cusabio |
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Description: A polyclonal antibody against DMD. Recognizes DMD from Human. This antibody is FITC conjugated. Tested in the following application: ELISA |
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![]() DMD Antibody, Biotin conjugated |
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1-CSB-PA006963LD01HU | Cusabio |
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Description: A polyclonal antibody against DMD. Recognizes DMD from Human. This antibody is Biotin conjugated. Tested in the following application: ELISA |
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![]() Anti-Dystrophin/DMD Antibody |
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PB9276 | BosterBio | 100ug/vial | 400.8 EUR |
![]() DMD cloning plasmid |
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CSB-CL006963HU-10ug | Cusabio | 10ug | 772.8 EUR |
Description: A cloning plasmid for the DMD gene. |
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![]() Recombinant Dystrophin (DMD) |
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4-RPB503Hu01 | Cloud-Clone |
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Description: Recombinant Human Dystrophin expressed in: E.coli |
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![]() Recombinant Dystrophin (DMD) |
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4-RPB503Mu01 | Cloud-Clone |
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Description: Recombinant Mouse Dystrophin expressed in: E.coli |
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![]() Mouse DMD shRNA Plasmid |
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20-abx970021 | Abbexa |
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![]() Human DMD shRNA Plasmid |
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20-abx951219 | Abbexa |
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![]() Mouse DMD ELISA Kit |
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EMD0036 | Abclonal | 96Tests | 625.2 EUR |
DMD Rabbit Polyclonal Antibody