ACTA1 Monoclonal Antibody

Background:
This gene encodes a member of a subfamily of the adenosine deaminase protein family. The encoded protein is one of two adenosine deaminases found in humans, which regulate levels of the signaling molecule, adenosine. The encoded protein is secreted from monocytes undergoing differentiation and may regulate cell proliferation and differentiation. This gene may be responsible for some of the phenotypic features associated with cat eye syndrome. Alternative splicing results in multiple transcript variants.
ADA2 (Adenosine Deaminase 2) is a Protein Coding gene. Diseases associated with ADA2 include Sneddon Syndrome and Polyarteritis Nodosa, Childhood-Onset. Among its related pathways are Innate Immune System and Metabolism of proteins.

Research Area: Cancer, Signal Transduction, Tags and Cell Markers

Synonyms:
a actin, ACTA, ACTA1, Actin alpha skeletal muscle, Actin, actin, alpha 1, skeletal muscle 1, actin, alpha 1, skeletal muscle, Actin, alpha skeletal muscle, actina, actine, ACTS, aktin, Alpha Actin 1, Alpha skeletal muscle Actin, alpha skeletal muscle, alpha-actin, Alpha-actin-1, ASMA, CFTD, CFTD1, CFTDM, MPFD, NEM1, NEM2, NEM3, nemaline myopathy type 3

Immunogen: Synthetic Peptide of Muscle actin

Swissprot: P68133

Purification Method: Protein A purification

Buffer: PBS with 0.02% sodium azide, 0.5% BSA and 50% glycerol, pH7.4

Concentration: 1 mg/mL
Dilution: IHC 1:100-200

Storage:
Store at -20°C. Avoid freeze / thaw cycles.