PKC gamma Polyclonal Antibody
规格: | / 20μL / 60μL / 120μL / 200μL |
价格: | / ¥420 / ¥1010 / ¥1640 / ¥2365 |
货号:E-AB-16194
宿主: Rabbit
反应性: H,M,R
应用: WB
Overview
Synonyms | KPCG,MGC57564,OTTHUMP00000067291,PKC-gamma,PKCC,PKCG,PRKCG,Protein kinase C gamma,Protein kinase C gamma polypeptide,Protein kinase C gamma type,Protein kinase C,gamma,SCA 14,SCA14,PRKCG抗体 |
Swissprot | P05129 |
Source | Rabbit |
Reactivity | Human,Mouse,Rat |
Immunogen | Synthetic peptide of human PRKCG |
Application | WB(Detection kit: E-IR-R304) |
Recommended dilution | WB,,1:500-1:2000; |
Concentration | 0.7 mg/mL |
Clonality | Polyclonal |
Properties
Cellular localization | Cytosol,Nucleus,Plasma Membrane,synaptic membrane,Other locations:cell-cell junction,dendrite,intracellular,perinuclear region of cytoplasm,postsynaptic density |
Tissue specificity | Expressed in Purkinje cells of the cerebellar cortex. |
Isotype | IgG |
Purification | Affinity purification |
Conjugation | Unconjugated |
Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
Storage buffer | PBS with 0.05% sodium azide, 50% glycerol, PH7.3 |
Background | Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play distinct roles in cells. The protein encoded by this gene is one of the PKC family members. This protein kinase is expressed solely in the brain and spinal cord and its localization is restricted to neurons. It has been demonstrated that several neuronal functions, including long term potentiation (LTP) and long term depression (LTD), specifically require this kinase. Knockout studies in mice also suggest that this kinase may be involved in neuropathic pain development. Defects in this protein have been associated with neurodegenerative disorder spinocerebellar ataxia-14 (SCA14) |