huntington Antibody
huntington Antibody
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abx031218-80l | Abbexa | 80 µl | EUR 286 |
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abx027897-400ul | Abbexa | 400 ul | EUR 523 |
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abx027897-80l | Abbexa | 80 µl | EUR 286 |
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AF4659 | Affbiotech | 200ul | EUR 376 |
Description: H2B Antibody Antibody detects endogenous levels of H2B. |
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ABD2911 | Lifescience Market | 100 ug | EUR 438 |
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LSMab09882 | Lifescience Market | 100 ug | EUR 438 |
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20-abx123734 | Abbexa |
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abx036399-100ug | Abbexa | 100 ug | EUR 391 |
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abx033330-400ul | Abbexa | 400 ul | EUR 523 |
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abx033330-80l | Abbexa | 80 µl | EUR 286 |
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20-abx008109 | Abbexa |
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20-abx004855 | Abbexa |
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20-abx014333 | Abbexa |
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20-abx324434 | Abbexa |
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20-abx319900 | Abbexa |
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20-abx319901 | Abbexa |
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20-abx319905 | Abbexa |
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20-abx319913 | Abbexa |
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20-abx311665 | Abbexa |
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abx234901-100ug | Abbexa | 100 ug | EUR 551 |
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abx230204-100ug | Abbexa | 100 ug | EUR 481 |
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STJ28365 | St John's Laboratory | 100 µl | EUR 277 |
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STJ28963 | St John's Laboratory | 100 µl | EUR 277 |
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19. |
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STJ11100949 | St John's Laboratory | 100 µl | EUR 277 |
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined. |
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STJ25475 | St John's Laboratory | 100 µl | EUR 277 |
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STJ25477 | St John's Laboratory | 100 µl | EUR 277 |
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced. |
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STJ25479 | St John's Laboratory | 100 µl | EUR 277 |
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. |
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STJ111369 | St John's Laboratory | 100 µl | EUR 277 |
Description: This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described. |
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STJ111530 | St John's Laboratory | 100 µl | EUR 277 |
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STJ112276 | St John's Laboratory | 100 µl | EUR 277 |
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is highly expressed in brain and heart. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. One of the isoforms (known as ARTS) is distinct; it is localized to the mitochondria, and has a role in apoptosis and cancer. |
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STJ112609 | St John's Laboratory | 100 µl | EUR 277 |
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STJ113941 | St John's Laboratory | 100 µl | EUR 277 |
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STJ114081 | St John's Laboratory | 100 µl | EUR 277 |
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STJ114819 | St John's Laboratory | 100 µl | EUR 277 |
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced. |
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STJ114828 | St John's Laboratory | 100 µl | EUR 277 |
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STJ118549 | St John's Laboratory | 100 µl | EUR 277 |
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STJ118550 | St John's Laboratory | 100 µl | EUR 277 |
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STJ118752 | St John's Laboratory | 100 µl | EUR 277 |
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STJ118990 | St John's Laboratory | 100 µl | EUR 277 |
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STJ119580 | St John's Laboratory | 100 µl | EUR 277 |
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis and the maintenance of cellular morphology. This gene encodes a protein that can form homo- and heterooligomeric filaments, and may contribute to the formation of neurofibrillary tangles in Alzheimer's disease. Alternatively spliced transcript variants have been found but the full-length nature of these variants has not been determined. [provided by RefSeq, Dec 2012] |
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STJ116214 | St John's Laboratory | 100 µl | EUR 277 |
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19. |
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STJ117206 | St John's Laboratory | 100 µl | EUR 277 |
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. |
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STJ117759 | St John's Laboratory | 100 µl | EUR 277 |
Description: This gene encodes a guanine-nucleotide binding protein and member of the septin family of cytoskeletal GTPases. Septins play important roles in cytokinesis, exocytosis, embryonic development, and membrane dynamics. Multiple transcript variants encoding different isoforms have been found for this gene. |
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AMM06679G | Leading Biology | 0.05mg | EUR 528 |
Description: A Monoclonal antibody against Human NGF/proNGF Neutralizing. The antibodies are raised in Mouse. This antibody is applicable in E |
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20-abx103034 | Abbexa |
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20-abx103035 | Abbexa |
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20-abx103036 | Abbexa |
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abx023924-1mg | Abbexa | 1 mg | EUR 1205 |
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20-abx319902 | Abbexa |
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20-abx319903 | Abbexa |
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20-abx319904 | Abbexa |
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20-abx319906 | Abbexa |
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20-abx319907 | Abbexa |
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20-abx319908 | Abbexa |
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20-abx319914 | Abbexa |
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20-abx319915 | Abbexa |
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20-abx319916 | Abbexa |
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20-abx319929 | Abbexa |
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20-abx319930 | Abbexa |
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20-abx319931 | Abbexa |
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20-abx311666 | Abbexa |
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20-abx311667 | Abbexa |
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20-abx311668 | Abbexa |
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abx411057-50ug | Abbexa | 50 ug | EUR 592 |
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abx233571-100ug | Abbexa | 100 ug | EUR 481 |
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48169-100ul | SAB | 100ul | EUR 333 |
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48169-50ul | SAB | 50ul | EUR 239 |
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065-A-01mg | Virogen | 0,1 mg | EUR 267.5 |
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Description: anti-CD22 monoclonal antibody |
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065-A-1000ug | Virogen | 1000 ug | EUR 1282.5 |
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Description: anti-CD22 monoclonal antibody |
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10R-1876 | Fitzgerald | 100 ul | EUR 651 |
Description: Mouse monoclonal Antibody Pair to ApoA-V antibody |