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Anti-ATP6V1B1 TRUEMAB Antibody clone 2D2
TrueMAB Antibodies - Made against Authentic Protein Antigens
Also for ATP6V1B1 (NM_001692)
|Full length human recombinant protein of human ATP6V1B1 (NP_001683) produced in HEK293T cell.|
|WB, IF, FC
||WB 1:500~2000, IF 1:100, FLOW 1:100
|PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.|
|Purified from mouse ascites fluids by affinity chromatography (Protein A or G Sepharose)
|Homo sapiens ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1 (ATP6V1B1)|
|ATP6B1; RTA1B; VATB; VMA2; VPP3|
|This gene 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 and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of two V1 domain B subunit isoforms and is found in the kidney. Mutations in this gene cause distal renal tubular acidosis associated with sensorineural deafness. [provided by RefSeq]. |
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HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY ATP6V1B1 (RC209462, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-ATP6V1B1.
Anti-ATP6V1B1 mouse monoclonal antibody (TA502667) immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY ATP6V1B1(RC209462 ).
HEK293T cells transfected with either RC209462 overexpress plasmid(Red) or empty vector control plasmid(Blue) were immunostained by anti-ATP6V1B1 antibody(TA502667), and then analyzed by flow cytometry.
Flow cytometric Analysis of Hela cells, using anti-ATP6V1B1 antibody(TA502667),(Red), compared to a nonspecific negative control antibody(TA50011),(Blue).
Flow cytometric Analysis of Jurkat cells, using anti-ATP6V1B1 antibody(TA502667),(Red), compared to a nonspecific negative control antibody(TA50011),(Blue).