ATP6V1B2 Antibody

Code CSB-PA002398ESR1HU
Size US$299Purchase it in Cusabio online store
(only available for customers from the US)
  • Western blot
    All lanes: ATP6V1B2 antibody at 5µg/ml + Hela whole cell lysate
    Goat polyclonal to rabbit IgG at 1/10000 dilution
    Predicted band size: 57 kDa
    Observed band size: 57 kDa

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Product Details

Full Product Name Rabbit anti-Homo sapiens (Human) ATP6V1B2 Polyclonal antibody
Uniprot No. P21281
Target Names ATP6V1B2
Alternative Names ATP6B1B2 antibody; ATP6B2 antibody; ATP6V1 B2 antibody; ATP6V1B 2 antibody; ATP6V1B2 antibody; ATPase H+ transporting lysosomal 56/58kDa V1 subunit B isoform 2 antibody; ATPase H+ transporting lysosomal 56/58kDa V1 subunit B2 antibody; ATPase H+ transporting, lysosomal (vacuolar proton pump) beta polypeptide 56/58kD isoform 2 antibody; ATPase, H+ transporting, lysosomal V1 subunit B2 antibody; brain isoform antibody; Endomembrane proton pump 58 kDa subunit antibody; H+ transporting two sector ATPase antibody; HO 57 antibody; HO57 antibody; V ATPase B2 subunit antibody; V ATPase subunit B 2 antibody; V type proton ATPase subunit B, brain isoform antibody; V-ATPase subunit B 2 antibody; V-type proton ATPase subunit B antibody; Vacuolar ATP synthase subunit B brain isoform antibody; Vacuolar H+ ATPase 56,000 subunit antibody; Vacuolar H+ ATPase 56000 subunit antibody; Vacuolar H+ATPase B2 antibody; Vacuolar proton pump subunit B 2 antibody; VAT B2 antibody; VATB 2 antibody; VATB antibody; VATB2 antibody; VATB2_HUMAN antibody; Vma 2 antibody; Vma2 antibody; VPP 3 antibody; VPP3 antibody
Raised in Rabbit
Species Reactivity Human
Immunogen Recombinant Human V-type proton ATPase subunit B, brain isoform protein (262-511AA)
Immunogen Species Homo sapiens (Human)
Conjugate Non-conjugated
Clonality Polyclonal
Isotype IgG
Purification Method Antigen Affinity Purified
Concentration It differs from different batches. Please contact us to confirm it.
Buffer PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Form Liquid
Tested Applications ELISA, WB
Recommended Dilution
Application Recommended Dilution
WB 1:1000-1:5000
Protocols ELISA Protocol
Western Blotting(WB) Protocol
Troubleshooting and FAQs Antibody FAQs
Storage Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Non-catalytic subunit of the V1 complex of vacuolar(H+)-ATPase (V-ATPase), a multisubunit enzyme composed of a peripheral complex (V1) that hydrolyzes ATP and a membrane integral complex (V0) that translocates protons. V-ATPase is responsible for acidifying and maintaining the pH of intracellular compartments and in some cell types, is targeted to the plasma membrane, where it is responsible for acidifying the extracellular environment. In renal intercalated cells, can partially compensate the lack of ATP6V1B1 and mediate secretion of protons (H+) into the urine under base-line conditions but not in conditions of acid load.
Gene References into Functions
  1. We conclude that the effects of variation in the vacuolar ATPase may point to a new molecular mechanism that influences the long-term development of depression. This mechanism may involve dysfunction specifically in hippocampal circuitry and cognitive impairment that characterizes recurrent and chronic depression. PMID: 27824360
  2. ATP6V1B2 is somatically mutated in 22% of follicular lymphoma tumors. Mutation hotspots found at Y371 and R400. PMID: 25713363
  3. A missense mutation in ATP6V1B2 associated with Zimmermann-Laband syndrome. PMID: 25915598
  4. The ATP6V1B2 p.Arg506X is a haploinsufficient mutation and resulted in abnormal acidification in lysosomes. PMID: 24913193
  5. This protein has been found differentially expressed in the anterior cingulate cortex from patients with schizophrenia PMID: 20381070

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Involvement in disease Zimmermann-Laband syndrome 2 (ZLS2); Deafness, congenital, with onychodystrophy, autosomal dominant (DDOD)
Subcellular Location Apical cell membrane. Melanosome. Cytoplasm.
Protein Families ATPase alpha/beta chains family
Tissue Specificity Kidney; localizes to early distal nephron, encompassing thick ascending limbs and distal convoluted tubules (at protein level).
Database Links

HGNC: 854

OMIM: 124480

KEGG: hsa:526

STRING: 9606.ENSP00000276390

UniGene: Hs.295917


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