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The antibody against ATP6V0A1 was raised in rabbit using the Recombinant Human V-type proton ATPase 116 kDa subunit a isoform 1 protein (80-260AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB, IHC, IF.
The antibody against ATP6V0A1 was raised in rabbit using the Recombinant Human V-type proton ATPase 116 kDa subunit a isoform 1 protein (80-260AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB, IHC, IF.
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| Cat.No | ADC-09534A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | ATP6V0A1 |
| Target Synonyms | H+ transporting, lysosomal | Form | Liquid |
| Species Reactivity | Human, Mouse, Rat | Isotype | IgG |
| Storage Buffer | 0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4 | Purification Method | >95%, Protein G purified |
| Conjugate | Non-conjugated | Application | ELISA, IF, IHC, WB |
| Storage | Upon receipt |
| Immunogen Description | Recombinant Human V-type proton ATPase 116 kDa subunit a isoform 1 protein (80-260AA) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | Q93050 |
Uniprot Id
Q93050
Target Species
Human
Target Name
ATP6V0A1
Target Full Name
V-type proton ATPase 116 kDa subunit a 1
Target Function
Required for assembly and activity of the vacuolar ATPase. Potential role in differential targeting and regulation of the enzyme for a specific organelle.
Target Subcellular Location
Cytoplasmic vesicle membrane; Multi-pass membrane protein. Melanosome. Note=Coated vesicle. Identified by mass spectrometry in melanosome fractions from stage I to stage IV.
Target Protein Families
V-ATPase 116 kDa subunit family
Target Synonyms
a1; ATP6N1; ATP6N1A; ATP6V0A1; 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); ATPase H+ transporting lysosomal V0 subunit a1; ATPase H+ transporting V0 subunit a1; ATPase, H+ transporting, lysosomal, noncatalytic accessory protein 1A; Clathrin coated vesicle/synaptic vesicle proton pump 116 kDa subunit; Clathrin-coated vesicle/synaptic vesicle proton pump 116 kDa subunit; DKFZp781J1951; H(+) transporting two sector ATPase 116 kDa accessory protein A1; Stv1; V ATPase 116 kDa; V ATPase 116 kDa isoform a1; V type proton ATPase 116 kDa subunit a; V type proton ATPase 116 kDa subunit a isoform 1; V-ATPase 116 kDa isoform a1; V-type proton ATPase 116 kDa subunit a isoform 1; Vacuolar adenosine triphosphatase subunit Ac116; Vacuolar proton pump subunit 1; Vacuolar proton pump, subunit 1; Vacuolar proton translocating ATPase 116 kDa subunit A; Vacuolar proton translocating ATPase 116 kDa subunit a isoform 1; Vacuolar type H(+) ATPase 115 kDa subunit; Vph1; VPP1; VPP1_HUMAN
Target Background
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.
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