Cell Signaling Technology

Product Pathways - PI3K / Akt Signaling

ATP6V1B2 (D3O7Q) Rabbit mAb #14488

ATP6B1B2   ATP6B2   ATPase. H+ transporting. lysosomal 56/58kDa. V1 subunit B2   Endomembrane proton pump 58 kDa subunit   H+ transporting two-sector ATPase   HO57   V-ATPase B2 subunit   V-ATPase subunit B 2   V-type proton ATPase subunit B. brain isoform   vacuolar H+-ATPase 56.000 subunit   Vacuolar proton pump subunit B 2   VATB   VATB2   Vma2   VPP3  

No. Size Price
14488S 100 µl ( 10 western blots ) ¥3,100.00 现货查询 购买询价
14488 carrier free & custom formulation / quantityemail request
Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
W 1:1000 Human,Mouse,Rat,Monkey, Endogenous 55 Rabbit IgG
IP 1:50

Species cross-reactivity is determined by western blot.

Applications Key: W=Western Blotting, IP=Immunoprecipitation,

Specificity / Sensitivity

ATP6V1B2 (D3O7Q) Rabbit mAb recognizes endogenous levels of total ATP6V1B2 protein. This antibody does not cross-react with ATP6V1B1 protein.

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the amino terminus of human ATP6V1B2 protein.

Western Blotting

Western Blotting

Western blot analysis of extracts from various cell lines using ATP6V1B2 (D3O7Q) Rabbit mAb.


Eukaryotic cells contain ATP-driven proton pumps known as vacuolar H+-ATPases (V-ATPases) that acidify intracellular compartments and translocate protons across the plasma membrane (1,2). Intracellular v-ATPases play an important role in endocytosis and intracellular membrane trafficking, while plasma membrane v-ATPases are important in processes such as urinary acidification and bone resorption (1,2). Vacuolar ATPase enzymes are large, heteromultimeric protein complexes with component proteins found in either the V1 peripheral domain or the V0 integral domain (2). The cytoplasmic V1 domain contains a hexamer of A and B catalytic subunits, as well as a number of other protein subunits required for ATPase assembly and ATP hydrolysis. The integral V0 v-ATPase domain exhibits protein translocase activity and is responsible for transport of protons across the membrane (2). Research studies show that the v-ATPases ATP6V0c, ATP6V0d1, ATP6V1A, ATP6V1B2, and ATP6V1D interact with the Ragulator protein complex and are essential for amino acid induced activation of mTORC1 on the surface of lysosomes (3).

Two isoforms of the B subunit are found in humans, ATP6V1B1 and ATP6V1B2. The ATP6V1B1 protein is expressed primarily in the kidney, with mutations in the corresponding gene responsible for a form of renal tubular acidosis associated with progressive hearing loss (4,5). ATP6V1B2 protein exhibits a broader range of expression, localized to kidney, brain, pancreas, and other tissues (4).

  1. Marshansky, V. and Futai, M. (2008) Curr Opin Cell Biol 20, 415-26.
  2. Jefferies, K.C. et al. (2008) Arch Biochem Biophys 476, 33-42.
  3. Zoncu, R. et al. (2011) Science 334, 678-83.
  4. van Hille, B. et al. (1994) Biochem J 303 ( Pt 1), 191-8.
  5. Karet, F.E. et al. (1999) Nat Genet 21, 84-90.

Application References

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