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cAMP Protein Kinase Catalytic subunit Recombinant Rabbit mAb

Cat No.: RMA02036
规格:
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  • Western blot analysis of Anti-cAMP Protein Kinase Catalytic subunit antibody(RMA02036) Gel: 10% SDS-PAGE Lysate: 20 μg Primary antibody: RMA02036(cAMP Protein Kinase Catalytic subunit antibody)at dilution 1:1000 Secondary antibody: Goat anti rabbit IgG (SPA10002)at 1:1000 dilution

Product Name: cAMP Protein Kinase Catalytic subunit Recombinant Rabbit mAb
Cat No.: RMA02036
Clonality: Monoclonal
Species Reactivity: Human, Mouse, Rat
Tested Applications: WB,IHC,ICC/IF,FC,IP
Recommended Dilution: WB,IHC,ICC/IF,FC,IP
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 peptide of human cAMP Protein Kinase Catalytic subunit
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
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