| Product name | VATB2 Polyclonal Antibody |
| Immunogen | Synthesized peptide derived from part region of human VATB2 protein |
| Host | Rabbit |
| Reactivity | Human,Rat,Mouse,Swine |
| Applications | WB,ELISA |
| Applications notes | Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000;ELISA 1:5000-20000 |
| Clonality | Polyclonal |
| Preparation method | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
| Alternative | V-type proton ATPase subunit B, brain isoform; V-ATPase subunit B 2; Endomembrane proton pump 58 kDa subunit; HO57; Vacuolar proton pump subunit B 2 |
| Formulation | Liquid solution |
| Concentration | 1 mg/ml |
| Molecular weight | 56kD |
| Storage buffer | PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA |
| Storage instructions | Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing. |
| Shipping | Gel pack with blue ice. |
| Precautions | The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product. |
| Background | ATP6V1B2 (ATPase H+ Transporting V1 Subunit B2) is a Protein Coding gene. Diseases associated with ATP6V1B2 include Zimmermann-Laband Syndrome 2 and Deafness, Congenital, With Onychodystrophy, Autosomal Dominant. Among its related pathways are Rheumatoid arthritis and mTOR signaling pathway (KEGG). ATP6V1B2 encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A, three B, and two G subunits, as well as a C, D, E, F, and H subunit. The V1 domain contains the ATP catalytic site. The protein encoded by ATP6V1B2 is one of two V1 domain B subunit isoforms and is the only B isoform highly expressed in osteoclasts. |
| Gene ID | 526 |
| Alternative | V-type proton ATPase subunit B, brain isoform; V-ATPase subunit B 2; Endomembrane proton pump 58 kDa subunit; HO57; Vacuolar proton pump subunit B 2 |
| Others | The antibody detects endogenous levels of VATB2 protein |
| Accession | P21281 |
| Observed Band(KD) | 56 |
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