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- goat polyclonal IgG, 200µg/ml
- epitope mapping within an internal region of BPGM of human origin
- recommended for detection of BPGM of mouse, rat and human origin by WB, IP, IF and ELISA; also reactive with additional species, including equine, canine and bovine
- blocking peptide, sc-82786 P
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Información sobre pedidos
Productos Recomendados para Ayudar:
(Haga clic en el botón para el applicación de su selección)
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| Especie |
Nombre del Gen |
Identificacion del Gen |
Ubicacion del cromosoma |
Numero de Accesion de Isoforma (ARNm) |
Numero de Accesion de la Proteina |
Número de pedido: |
| Humano |
BPGM |
669 |
7q33 |
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P07738
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222800 |
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BPGM Background Information
BPGM (2,3-bisphosphoglycerate mutase) is a 259 amino acid protein that belongs to the phosphoglycerate mutase family and exists as a homodimer that plays a crucial role in the regulation of hemoglobin oxygen. Specifically, BPGM catalyzes the conversion of 3-phospho-D-glyceroyl phosphate to 2,3-bisphospho-D-glycerate (2,3-BPG), a reaction that is essential for controlling the concentration of 2,3-BPG within the cell. The gene encoding BPGM maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. |
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BPGM (L-15)
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BPGM (L-15): sc-82786. Western blot analysis of BPGM expression in human erythrocyte whole cell lysate.
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