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anti-Human ATP6V0A1 Antibodies:
anti-Mouse (Murine) ATP6V0A1 Antibodies:
anti-Rat (Rattus) ATP6V0A1 Antibodies:
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Human Polyclonal ATP6V0A1 Primary Antibody for ELISA, WB - ABIN560006
Chasiotis, Ionescu, Misyura, Bui, Fazio, Wang, Patrick, Weihrauch, Donini: An animal homolog of plant Mep/Amt transporters promotes ammonia excretion by the anal papillae of the disease vector mosquito Aedes aegypti. in The Journal of experimental biology 2016
Cow (Bovine) Polyclonal ATP6V0A1 Primary Antibody for WB - ABIN2782670
Antonacopoulou, Grivas, Skarlas, Kalofonos, Scopa, Kalofonos: POLR2F, ATP6V0A1 and PRNP expression in colorectal cancer: new molecules with prognostic significance? in Anticancer research 2008
Show all 2 Pubmed References
Human Polyclonal ATP6V0A1 Primary Antibody for ICC, IF - ABIN4282299
Bagh, Peng, Chandra, Zhang, Singh, Pattabiraman, Liu, Mukherjee: Misrouting of v-ATPase subunit V0a1 dysregulates lysosomal acidification in a neurodegenerative lysosomal storage disease model. in Nature communications 2017
The function of vacuolar ATPase (V-ATPase) a subunit isoforms in invasiveness of MCF10a and MCF10CA1a human breast cancer cells.
Inhibition of lysosome degradation on autophagosome formation and responses to GMI, an immunomodulatory protein from Ganoderma microsporum. ATP6V0A1 plays an important role in mediating autophagosome-lysosome fusion.
a series of events whereby ATP6V0A1 3'-UTR variant T+3246C functioned: ATP6V0A1 expression probably was affected through differential micro-RNA effects, altering vacuolar pH and consequently CHGA processing and exocytotic secretion.
The mRNA levels of POLR2F, ATP6V0A1 and PRNP were evaluated by quantitative RT-PCR in 70 colorectal carcinomas and 17 normal tissue specimens and were correlated with clinicopathological parameters.
These results suggest that the Golgi complex may serve as a membrane platform for noncanonical autophagy where V-ATPase is a key player.
Data suggest a mechanism by which betaA3/A1-crystallin regulates lysosomal function by modulating the activity of V-ATPase.
demonstrated that CRYBA1 coimmunoprecipitates with the ATP6V0A1/V0-ATPase a1 subunit
V-ATPase membrane domain would allow the exocytotic machinery to discriminate fully loaded and acidified vesicles from vesicles undergoing neurotransmitter reloading.
Immunolocalization demonstrated expression of all 'a' subunits in the proximal tubule and in the intercalated cells of the collecting system. PCR detected mRNAs encoding all four 'a' isoforms with a relative abundance in the following order: a4>a2=a1>a3.
In vivo imaging of living brains reveals that digestion of neurons occurs in compartments arising from the progressive fusion of vesicles and demonstrates that this fusion is mediated by the v0-ATPase a1 subunit.
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 gene encodes one of three A subunit proteins and the encoded protein is associated with clathrin-coated vesicles. Three transcript variants encoding different isoforms have been found for this gene.
ATPase, H+ transporting, lysosomal (vacuolar proton pump) non-catalytic accessory protein 1A (110/116kD)
, ATPase, H+ transporting, lysosomal non-catalytic accessory protein 1 (110/116kD)
, H(+)-transporting two-sector ATPase, 116 kDa accessory protein A1
, V-ATPase 116 kDa
, V-type proton ATPase 116 kDa subunit a
, V-type proton ATPase 116 kDa subunit a isoform 1
, clathrin-coated vesicle/synaptic vesicle proton pump 116 kDa subunit
, vacuolar adenosine triphosphatase subunit Ac116
, vacuolar proton pump subunit 1
, vacuolar proton pump, subunit 1
, vacuolar proton translocating ATPase 116 kDa subunit A
, vacuolar-type H(+)-ATPase 115 kDa subunit
, ATPase, H+ transporting, lysosomal (vacuolar proton pump) noncatalytic accessory protein 1 (110/160 kDa)
, ATPase, H+ transporting, lysosomal (vacuolar proton pump) noncatalytic accessory protein 1A (110/160 kDa)
, ATPase, H+ transporting, lysosomal V0 subunit a
, V-ATPase a1
, vacuolar proton translocating ATPase 116 kDa subunit a
, ATPase H+ transporting lysosomal (vacuolar proton pump) noncatalytic accessory protein 1 (110/160 kDa)
, ATPase, H+ transporting, lysosomal noncatalytic accessory protein 1a
, v-H+ATPase subunit a1
, vacuolar H(+)-transporting ATPase 116 kDa subunit, a1 isoform