ATP6V1G2 anticorps (AA 51-118)

N° du produit ABIN6942179

Détail du produit anti-ATP6V1G2 anticorps

Antigène: ATP6V1G2 (ATPase, H+ Transporting, Lysosomal 13kDa, V1 Subunit G2 (ATP6V1G2))

Épitope: AA 51-118

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ATP6V1G2 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)

Réactivité croisée: Souris, Rat

Homologie: Human,Dog,Cow,Sheep,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human ATP6V1G2

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur ATP6V1G2

Antigène: ATP6V1G2 (ATPase, H+ Transporting, Lysosomal 13kDa, V1 Subunit G2 (ATP6V1G2))

Autre désignation: ATP6V1G2 (ATP6V1G2 Produits)

Synonymes: anticorps ATP6G, anticorps ATP6V1G1, anticorps ATP6G2, anticorps NG38, anticorps VMA10, anticorps ATP6G1, anticorps 1500002D01Rik, anticorps Atp6g2, anticorps VAG2, anticorps ATPase H+ transporting V1 subunit G2, anticorps ATPase, H+ transporting, lysosomal V1 subunit G2, anticorps ATP6V1G2, anticorps Atp6v1g2

Sujet:

Synonyms: ATP6G, ATP6G2, ATPase H+ transporting lysosomal (vacuolar proton pump) subunit G, ATPase H+ transporting lysosomal 13 kDa V1 subunit G2, H(+) transporting two sector ATPase subunit G2, NG 38, NG38, V ATPase 13 kDa subunit 2, V ATPase G subunit 2, V ATPase subunit G 2, Vacuolar ATP synthase subunit G 2, Vacuolar proton pump G subunit 2, Vacuolar proton pump subunit G 2, VMA 10, VMA10.

Background: This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent 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 three V1 domain G subunit proteins. This gene had previous gene symbols of ATP6G and ATP6G2. Alternatively spliced transcript variants encoding different isoforms have been described. Read-through transcription also exists between this gene and the downstream DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B (DDX39B) gene. [provided by RefSeq, Feb 2011]

ID gène: 534

UniProt: O95670

Pathways: Transition Metal Ion Homeostasis, Proton Transport