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Mouse Anti-CA5A Recombinant Antibody (MM0676-7S19) (CBMAB-C9588-LY)

The product is antibody recognizes CA5A. The antibody MM0676-7S19 immunoassay techniques such as: WB, ELISA, IHC-P.
See all CA5A antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
MM0676-7S19
Antibody Isotype
IgG2
Application
WB, ELISA, IHC-P

Basic Information

Specificity
Human
Antibody Isotype
IgG2
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Concentration
0.2 mg/mL
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Full Name
Carbonic Anhydrase 5A
Introduction
Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. CA VA is localized in the mitochondria and expressed primarily in the liver. It may play an important role in ureagenesis and gluconeogenesis. CA5A gene maps to chromosome 16q24.3 and an unprocessed pseudogene has been assigned to 16p12-p11.2. [provided by RefSeq, Jul 2008]
Entrez Gene ID
763
UniProt ID
P35218
Alternative Names
Carbonic Anhydrase 5A; Carbonic Anhydrase VA, Mitochondrial; Carbonate Dehydratase VA; EC 4.2.1.1; CA-VA; CA5; Carbonic Anhydrase 5A, Mitochondrial; Carbonic Anhydrase V, Mitochondrial;
Function
Reversible hydration of carbon dioxide. Low activity.
Biological Process
Bicarbonate transport Source: Reactome
One-carbon metabolic process Source: GO_Central
Cellular Location
Mitochondrion
Involvement in disease
Hyperammonemia due to carbonic anhydrase VA deficiency (CA5AD): An autosomal recessive inborn error of metabolism, clinically characterized by infantile hyperammonemic encephalopathy. Metabolic abnormalities include hypoglycemia, hyperlactatemia, metabolic acidosis and respiratory alkalosis.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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