DMD Rabbit Polyclonal Antibody

DMD Rabbit Polyclonal Antibody

 

Mouse Dystrophin (DMD) ELISA Kit

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.

Human Dystrophin (DMD) ELISA Kit

RD-DMD-Hu-48Tests Reddot Biotech 48 Tests 600 EUR

Human Dystrophin (DMD) ELISA Kit

RD-DMD-Hu-96Tests Reddot Biotech 96 Tests 830.4 EUR

Mouse Dystrophin (DMD) ELISA Kit

RD-DMD-Mu-48Tests Reddot Biotech 48 Tests 613.2 EUR

Mouse Dystrophin (DMD) ELISA Kit

RD-DMD-Mu-96Tests Reddot Biotech 96 Tests 850.8 EUR

Human Dystrophin (DMD) ELISA Kit

RDR-DMD-Hu-48Tests Reddot Biotech 48 Tests 626.4 EUR

Human Dystrophin (DMD) ELISA Kit

RDR-DMD-Hu-96Tests Reddot Biotech 96 Tests 868.8 EUR

Mouse Dystrophin (DMD) ELISA Kit

RDR-DMD-Mu-48Tests Reddot Biotech 48 Tests 640.8 EUR

Mouse Dystrophin (DMD) ELISA Kit

RDR-DMD-Mu-96Tests Reddot Biotech 96 Tests 890.4 EUR

DMD Polyclonal Antibody

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

DMD Polyclonal Antibody

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

DMD Polyclonal Antibody

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

DMD Polyclonal Antibody

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

DMD Polyclonal Antibody

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

DMD Rabbit pAb

A1411-100ul Abclonal 100 ul 369.6 EUR

DMD Rabbit pAb

A1411-200ul Abclonal 200 ul 550.8 EUR

DMD Rabbit pAb

A1411-20ul Abclonal 20 ul 219.6 EUR

DMD Rabbit pAb

A1411-50ul Abclonal 50 ul 267.6 EUR

Polyclonal DMD / Dystrophin Antibody

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:

Rabbit DMD ELISA Kit

ERTD0036 Abclonal 96Tests 625.2 EUR

DMD Antibody

1-CSB-PA503789 Cusabio
  • 380.40 EUR
  • 292.80 EUR
  • 100ul
  • 50ul
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

DMD Antibody

1-CSB-PA006963GA01HU Cusabio
  • 716.40 EUR
  • 399.60 EUR
  • 150ul
  • 50ul
Description: A polyclonal antibody against DMD. Recognizes DMD from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB

DMD Antibody

1-CSB-PA006963LA01HU Cusabio
  • 380.40 EUR
  • 402.00 EUR
  • 100ug
  • 50ug
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

DMD antibody

70R-16862 Fitzgerald 50 ul 522 EUR
Description: Rabbit polyclonal DMD antibody

DMD Antibody

36428-100ul SAB 100ul 302.4 EUR

Dystrophin (DMD) Polyclonal Antibody (Human)

4-PAB503Hu01 Cloud-Clone
  • 286.80 EUR
  • 2869.20 EUR
  • 717.60 EUR
  • 358.80 EUR
  • 253.20 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD)

Dystrophin (DMD) Polyclonal Antibody (Mouse)

4-PAB503Mu01 Cloud-Clone
  • 291.60 EUR
  • 2948.40 EUR
  • 735.60 EUR
  • 366.00 EUR
  • 254.40 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD)

Rabbit Dystrophin (DMD) ELISA Kit

abx355333-96tests Abbexa 96 tests 990 EUR

DMD Conjugated Antibody

C36428 SAB 100ul 476.4 EUR

anti- DMD antibody

FNab02423 FN Test 100µg 606.3 EUR
Description: Antibody raised against DMD

Dystrophin (DMD) Antibody

20-abx100315 Abbexa
  • 393.60 EUR
  • 159.60 EUR
  • 944.40 EUR
  • 493.20 EUR
  • 309.60 EUR
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug

Dystrophin (DMD) Antibody

20-abx100316 Abbexa
  • 510.00 EUR
  • 159.60 EUR
  • 1412.40 EUR
  • 693.60 EUR
  • 393.60 EUR
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug

Dystrophin (DMD) Antibody

20-abx172180 Abbexa
  • 393.60 EUR
  • 978.00 EUR
  • 510.00 EUR
  • 184.80 EUR
  • 309.60 EUR
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug

Dystrophin (DMD) Antibody

20-abx149852 Abbexa
  • 510.00 EUR
  • 410.40 EUR
  • 100 ug
  • 50 ug

Dystrophin (DMD) Antibody

20-abx112214 Abbexa
  • 878.40 EUR
  • 477.60 EUR
  • 150 ul
  • 50 ul

Dystrophin (DMD) Antibody

20-abx001224 Abbexa
  • 493.20 EUR
  • 710.40 EUR
  • 218.40 EUR
  • 376.80 EUR
  • 100 ul
  • 200 ul
  • 20 ul
  • 50 ul

Dystrophin (DMD) Antibody

20-abx211560 Abbexa
  • 493.20 EUR
  • 360.00 EUR
  • 100 ul
  • 50 ul

Dystrophin (DMD) Antibody

abx232423-100ug Abbexa 100 ug 577.2 EUR

Dystrophin (DMD) Antibody

20-abx176215 Abbexa
  • 1412.40 EUR
  • 693.60 EUR
  • 1 mg
  • 200 ug

Anti-DMD antibody

PAab02423 Lifescience Market 100 ug 426 EUR

Anti-DMD antibody

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.

Anti-DMD antibody

STJ190175 St John's Laboratory 200 µl 236.4 EUR
Description: Unconjugated Rabbit polyclonal to DMD

Dystrophin Antibody / DMD

RQ5369 NSJ Bioreagents 100 ul 419 EUR

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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]

Dystrophin Antibody / DMD

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]

Dystrophin Antibody / DMD

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]

Dystrophin Antibody / DMD

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]

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin Antibody / DMD

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.

Dystrophin (DMD) Polyclonal Antibody (Human), APC

4-PAB503Hu01-APC Cloud-Clone
  • 399.60 EUR
  • 3735.60 EUR
  • 1046.40 EUR
  • 507.60 EUR
  • 258.00 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with APC.

Dystrophin (DMD) Polyclonal Antibody (Human), Biotinylated

4-PAB503Hu01-Biotin Cloud-Clone
  • 363.60 EUR
  • 2809.20 EUR
  • 836.40 EUR
  • 442.80 EUR
  • 259.20 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with Biotin.

Dystrophin (DMD) Polyclonal Antibody (Human), Cy3

4-PAB503Hu01-Cy3 Cloud-Clone
  • 483.60 EUR
  • 4930.80 EUR
  • 1345.20 EUR
  • 627.60 EUR
  • 294.00 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with Cy3.

Dystrophin (DMD) Polyclonal Antibody (Human), FITC

4-PAB503Hu01-FITC Cloud-Clone
  • 344.40 EUR
  • 3012.00 EUR
  • 860.40 EUR
  • 430.80 EUR
  • 230.40 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with FITC.

Dystrophin (DMD) Polyclonal Antibody (Human), HRP

4-PAB503Hu01-HRP Cloud-Clone
  • 366.00 EUR
  • 3256.80 EUR
  • 926.40 EUR
  • 459.60 EUR
  • 243.60 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with HRP.

Dystrophin (DMD) Polyclonal Antibody (Human), PE

4-PAB503Hu01-PE Cloud-Clone
  • 344.40 EUR
  • 3012.00 EUR
  • 860.40 EUR
  • 430.80 EUR
  • 230.40 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with PE.

Dystrophin (DMD) Polyclonal Antibody (Mouse), APC

4-PAB503Mu01-APC Cloud-Clone
  • 408.00 EUR
  • 3843.60 EUR
  • 1072.80 EUR
  • 518.40 EUR
  • 260.40 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with APC.

Dystrophin (DMD) Polyclonal Antibody (Mouse), Biotinylated

4-PAB503Mu01-Biotin Cloud-Clone
  • 368.40 EUR
  • 2888.40 EUR
  • 856.80 EUR
  • 450.00 EUR
  • 260.40 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with Biotin.

Dystrophin (DMD) Polyclonal Antibody (Mouse), Cy3

4-PAB503Mu01-Cy3 Cloud-Clone
  • 493.20 EUR
  • 5074.80 EUR
  • 1381.20 EUR
  • 642.00 EUR
  • 297.60 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with Cy3.

Dystrophin (DMD) Polyclonal Antibody (Mouse), FITC

4-PAB503Mu01-FITC Cloud-Clone
  • 350.40 EUR
  • 3098.40 EUR
  • 882.00 EUR
  • 439.20 EUR
  • 232.80 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with FITC.

Dystrophin (DMD) Polyclonal Antibody (Mouse), HRP

4-PAB503Mu01-HRP Cloud-Clone
  • 373.20 EUR
  • 3350.40 EUR
  • 949.20 EUR
  • 469.20 EUR
  • 246.00 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with HRP.

Dystrophin (DMD) Polyclonal Antibody (Mouse), PE

4-PAB503Mu01-PE Cloud-Clone
  • 350.40 EUR
  • 3098.40 EUR
  • 882.00 EUR
  • 439.20 EUR
  • 232.80 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with PE.

DMD siRNA

20-abx914266 Abbexa
  • 661.20 EUR
  • 878.40 EUR
  • 15 nmol
  • 30 nmol

DMD siRNA

20-abx914267 Abbexa
  • 661.20 EUR
  • 878.40 EUR
  • 15 nmol
  • 30 nmol

Dystrophin (DMD) Polyclonal Antibody (Human), APC-Cy7

4-PAB503Hu01-APC-Cy7 Cloud-Clone
  • 656.40 EUR
  • 7327.20 EUR
  • 1948.80 EUR
  • 872.40 EUR
  • 372.00 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with APC-Cy7.

Dystrophin (DMD) Polyclonal Antibody (Mouse), APC-Cy7

4-PAB503Mu01-APC-Cy7 Cloud-Clone
  • 672.00 EUR
  • 7543.20 EUR
  • 2002.80 EUR
  • 894.00 EUR
  • 378.00 EUR
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with APC-Cy7.

DMD Antibody, HRP conjugated

1-CSB-PA006963LB01HU Cusabio
  • 380.40 EUR
  • 402.00 EUR
  • 100ug
  • 50ug
Description: A polyclonal antibody against DMD. Recognizes DMD from Human. This antibody is HRP conjugated. Tested in the following application: ELISA

DMD Antibody, FITC conjugated

1-CSB-PA006963LC01HU Cusabio
  • 380.40 EUR
  • 402.00 EUR
  • 100ug
  • 50ug
Description: A polyclonal antibody against DMD. Recognizes DMD from Human. This antibody is FITC conjugated. Tested in the following application: ELISA

DMD Antibody, Biotin conjugated

1-CSB-PA006963LD01HU Cusabio
  • 380.40 EUR
  • 402.00 EUR
  • 100ug
  • 50ug
Description: A polyclonal antibody against DMD. Recognizes DMD from Human. This antibody is Biotin conjugated. Tested in the following application: ELISA

Anti-Dystrophin/DMD Antibody

PB9276 BosterBio 100ug/vial 400.8 EUR

DMD cloning plasmid

CSB-CL006963HU-10ug Cusabio 10ug 772.8 EUR
Description: A cloning plasmid for the DMD gene.

Recombinant Dystrophin (DMD)

4-RPB503Hu01 Cloud-Clone
  • 560.83 EUR
  • 273.60 EUR
  • 1773.12 EUR
  • 671.04 EUR
  • 1222.08 EUR
  • 451.20 EUR
  • 4252.80 EUR
  • 100 ug
  • 10ug
  • 1 mg
  • 200 ug
  • 500 ug
  • 50ug
  • 5 mg
Description: Recombinant Human Dystrophin expressed in: E.coli

Recombinant Dystrophin (DMD)

4-RPB503Mu01 Cloud-Clone
  • 582.34 EUR
  • 279.60 EUR
  • 1853.76 EUR
  • 697.92 EUR
  • 1275.84 EUR
  • 465.60 EUR
  • 4454.40 EUR
  • 100 ug
  • 10ug
  • 1 mg
  • 200 ug
  • 500 ug
  • 50ug
  • 5 mg
Description: Recombinant Mouse Dystrophin expressed in: E.coli

Mouse DMD shRNA Plasmid

20-abx970021 Abbexa
  • 961.20 EUR
  • 1345.20 EUR
  • 150 µg
  • 300 µg

Human DMD shRNA Plasmid

20-abx951219 Abbexa
  • 961.20 EUR
  • 1345.20 EUR
  • 150 µg
  • 300 µg

Mouse DMD ELISA Kit

EMD0036 Abclonal 96Tests 625.2 EUR

 

DMD Rabbit Polyclonal Antibody