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Porcine V-Type Proton ATPase Catalytic Subunit A (ATP6V1A) ELISA Kit-Sandwich

Cat. No.EK12F629

Product TypeAnimal Immunoassay Kits

Size

Product Overview

BioVenic Porcine V-Type Proton ATPase Catalytic Subunit A (ATP6V1A) ELISA Kit-Sandwich is designed for the quantitative determination of Porcine V-Type Proton ATPase Catalytic Subunit A (ATP6V1A) in serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids using a Sandwich ELISA method. For research use only.

Specifications

Assay Type ELISA-Sandwich
Specificity The assay kit is specific for Porcine ATP6V1A.
Target Species Swine
Species Reactivity Swine
Reproducibility Intra-Assay: CV < 10%; Inter-Assay: CV < 10%
Assay Time Around 270 min
Sample Requirement Serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids.

Target Information

V-Type Proton ATPase Catalytic Subunit A is encoded by the ATP6V1A gene in pigs. ATP6V1A is a component of the vacuolar ATPase (V-ATPase), a multisubunit enzyme. ATP6V1A is located in the V1 domain of the V-ATPase complex and is associated with many cellular biological processes in eukaryotic cells. It has been implicated in the dissociation of incoming viral M proteins during viral uncoating.

Target/Biomarker Porcine ATP6V1A
Target Synonym V-type proton ATPase catalytic subunit A; V-ATPase subunit A; V-ATPase 69 kDa subunit; Vacuolar proton pump subunit alpha; ATP6V1A; ATP6A1; ATP6V1A1; 3.6.3.14
Gene ID 445531
UniProt ID Q29048

Shipping and Storage

This product is shipped with gel ice packs. It is recommended to store at 2-8 °C (Up to 6 months).

Documents

COA

To request a Certificate of Analysis, please enter the Lot No. in the search box. Note: Certificate of Analysis not available for kits.

The product is for research use only.
Not for commercial, prophylactic, diagnostic, or therapeutic applications.

References

  1. Liu, X. et al. The ATPase ATP6V1A facilitates rabies virus replication by promoting virion uncoating and interacting with the viral matrix protein. The Journal of biological chemistry. 2021, 296: 100096.
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