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Phospho-PKC (Thr514) Recombinant Rabbit mAb

Cat No.: RMA02978
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  • Western blot analysis of Anti-Phospho-PKC (Thr514) antibody(RMA02978) Gel: 10% SDS-PAGE Lysate: 20 μg Primary antibody: RMA02978(Phospho-PKC (Thr514) antibody)at dilution 1:1000 Secondary antibody: Goat anti rabbit IgG (SPA10002)at 1:1000 dilution

Product Name: Phospho-PKC (Thr514) Recombinant Rabbit mAb
Cat No.: RMA02978
Clonality: Monoclonal
Species Reactivity: Human, Mouse, Rat
Tested Applications: WB,IHC,IP
Recommended Dilution: WB: 1:1000-1:5000
IHC: 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 Thr514 of human PKC
Calculated Molecular Weight: 78 kDa
Observed Molecular Weight: 78-85 kDa
GenBank Accession Number: P05129
Gene ID (NCBI): 5582
Synonyms: PKCC; PKCG; SCA14; PKC-gamma
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). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]
Category: Primary Ab
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