Recombinant Human PRKACA Protein
Cat#:TP03522应用:Positive Control; Immunogen; SDS-PAGE; WB
Product Name: | Phospho-PKA alpha/beta/gamma (catalytic subunit) (Thr197) Rabbit pAb |
Cat No.: | DPA05561 |
Clonality: | Polyclonal |
Species Reactivity: | Human, Mouse, Rat |
Tested Applications: | WB,IHC,ICC/IF,IP |
Recommended Dilution: | WB: 1:1000 IHC: 1:20-1:50 ICC/IF: 1:20-1:100 IP: 1:20 |
Size: | 30ul 50ul 100uL |
Format: | Liquid |
Source: | Rabbit |
Purification Method: | Affinity Purification |
Isotype: | IgG |
Conjugate: | Un-conjugated |
Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
Immunogen: | A synthetic phosphopeptide corresponding to residues surrounding Tyr197 of human PKA alpha/beta/gam |
Calculated Molecular Weight: | 41 kDa |
Observed Molecular Weight: | 41 kDa |
GenBank Accession Number: | P17612 |
Gene ID (NCBI): | 5566 |
Synonyms: | PKACA; PPNAD4 |
Background: | This gene encodes one of the catalytic subunits of protein kinase A, which exists as a tetrameric holoenzyme with two regulatory subunits and two catalytic subunits, in its inactive form. cAMP causes the dissociation of the inactive holoenzyme into a dimer of regulatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different regulatory subunits and three catalytic subunits have been identified in humans. cAMP-dependent phosphorylation of proteins by protein kinase A is important to many cellular processes, including differentiation, proliferation, and apoptosis. Constitutive activation of this gene caused either by somatic mutations, or genomic duplications of regions that include this gene, have been associated with hyperplasias and adenomas of the adrenal cortex and are linked to corticotropin-independent Cushing's syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. Tissue-specific isoforms that differ at the N-terminus have been described, and these isoforms may differ in the post-translational modifications that occur at the N-terminus of some isoforms. [provided by RefSeq, Jan 2015] |
Category: | Primary Ab |