Anti-ATP6V1A Antibody Picoband®

SKU: A10401-2

Size: 100 μg

Storage: At -20℃ for one year from date of receipt. After reconstitution, at 4℃ for one month. It can also be aliquotted and stored frozen at -20℃ for six months. Avoid repeated freezing and thawing.

Form: Lyophilized

Reactivity: Human,Mouse,Rat

Applications: WB,IHC,ICC,IF,Flow Cytometry,ELISA

Application Details: Western blot, 0.1-0.25 μg/ml, Human, Mouse, Rat
Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/ml, Human
Immunocytochemistry/Immunofluorescence, 5 μg/ml, Human
Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human
ELISA, 0.1-0.5 μg/ml, -

Gene Name: ATP6V1A

Specificity:

Background: V-type proton ATPase catalytic subunit A is an enzyme that in humans is encoded by the ATP6V1A gene. 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 A subunit isoforms and is found in all tissues. Transcript variants derived from alternative polyadenylation exist.

Immunogen: E.coli-derived human ATP6V1A recombinant protein (Position: R129-D617).

Clonality: Polyclonal

Contents: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Purification: Immunogen affinity purified.

Reconstitution: Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.

Reference: 1. Fassio, A., Esposito, A., Kato, M., Saitsu, H., Mei, D., Marini, C., Conti, V., Nakashima, M., Okamoto, N., Olmez Turker, A., Albuz, B., Semerci Gunduz, C. N., and 14 others. De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy. Brain 141: 1703-1718, 2018. 2. Gross, M. B. Personal Communication. Baltimore, Md. 1/3/2019. 3. Ramirez, C., Hauser, A. D., Vucic, E. A., Bar-Sagi, D. Plasma membrane V-ATPase controls oncogenic RAS-induced macropinocytosis. Nature 576: 477-481, 2019.

Uniprot ID: P38606

Host: Rabbit

Concentration: Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.

Conjugate:

Cross Reactivity: No cross-reactivity with other proteins.

Isotype: Rabbit IgG

Phospho_site:

Clone Number:

Observed Molecular Weight: 70 kDa

Calculated Molecular Weight: 41409 MW

Gene ID: 523

Protein Name: V-type proton ATPase catalytic subunit A

Gene Full Name: ATPase H+ transporting V1 subunit A

Synonyms: ATP6A1; ATP6V1A; ATP6V1A1; HO68; V ATPase 69 kDa subunit; V ATPase subunit A; VA68; Vacuolar ATPase isoform VA68; Vma1; VPP2