RECEIVE 25% OFF PUBLISHED ANTIBODIES WITH CODE "PUB25"! Offer valid for US customers and available internationally through distributors.

PKC_ (Central region) Antibody

Applications

  • WB
  • IP
  • IHC

Reactivity

  • Human
  • Mouse
  • Rat
Overview
Catalog # bsm-70611m
Product Name PKC_ (Central region) Antibody
Applications WB, IP, IHC
Specificity This antibody detects an 82kDa* protein corresponding to the molecular mass of PKC_ on SDS-PAGE immunoblots of neonatal rat brain and adult mouse brain lysates. This region is highly conserved in rat and mouse PKC_, and has homology to conserved regions in PKC_.
Reactivity Human, Mouse, Rat
Specifications
Conjugation Unconjugated
Host Mouse
Source Clone (M237) was generated from a recombinant human PKC_ that included amino acids residues in the central region.
Clonality Monoclonal
Clone # M237
Isotype IgG2b
Purification Purified by Protein A.
Storage Buffer PBS + 1 mg/ml BSA, 0.05% NaN3 and 50% glycerol
Storage Condition Storage at -20C is recommended, as aliquots may be taken without freeze/thawing due to presence of 50% glycerol. Stable for at least 1 year at -20C.
Target
Swiss Prot P17252
Synonyms PKC alpha
Background The Protein Kinase C (PKC) family of homologous serine/threonine protein kinases is involved in a number of processes such as growth, differentiation, and cytokine secretion. At least eleven isozymes have been described. PKC consists of a single polypeptide chain containing four conserved regions (C) and five variable regions (V). The N-terminal half interacts with PKC activators Ca2+, phospholipid, diacylglycerol, or phorbol ester, while the C-terminal half contains the catalytic domain. The conventional PKC subfamily (_, _1, _II, and _) is regulated by both Ca2+ and diacylglycerol. The PKC pathway represents a major signal transduction system that is activated following ligand-stimulation of transmembrane receptors by hormones, neurotransmitters and growth factors. The phosphorylation of multiple sites in conventional PKCs regulates their activity. In mast cells, FceRI stimulation leads to phosphorylation of tyrosine 658 and 662 of PKC_ and PKC_I respectively. This phosphorylation requires autophosphorylation of serine 657 and 661 in these respective kinases.
Application Dilution
WB
IP
IHC