PKC
Protein kinase C
PKC Isoform Specific Products
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PKC
(387)
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PKCα
(51)
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PKCβ
(43)
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PKCγ
(29)
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PKCδ
(29)
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PKCε
(33)
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PKCη
(15)
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PKCζ
(14)
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PKCθ
(21)
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PKCμ
(4)
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PKC-ι ℩
(2)
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PKCι
(7)
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PKC Related Products (512)
Related Products (512)
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Antibodies (21)
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PKC Isoform Comparison
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Protein Kinase C Peptide Substrate
0 ImagesCat. No.: HY-P1803CAS No.: 120253-69-2Synonyms: PKCε; PRKCE ; Peptide EpsilonProtein Kinase C Peptide Substrate is targeted to a specific cellular compartment in a manner dependent on second messengers and on specific adapter proteins in response to extracellular signals that activate G-protein-coupled receptors, tyrosine kinase receptors, or tyrosine kinase-coupled receptors. Protein Kinase C Peptide Substrate then regulates various physiological functions including the activation of nervous, endocrine, exocrine, inflammatory, and immune systems. -
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Ac-MBP (1-11)
0 ImagesCat. No.: HY-P1734CAS No.: 125366-42-9Ac-MBP 1-11, a short peptide sequence, is the major encephalitogenic epitope in myelin basic protein (MBP). -
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Chelerythrine chloride (Standard)
0 ImagesChelerythrine (chloride) (Standard) is the analytical standard of Chelerythrine (chloride). This product is intended for research and analytical applications. Chelerythrine chloride is a potent, cell-permeable inhibitor of protein kinase C, with an IC50 of 660 nM. Chelerythrine chloride inhibits the Bcl-XL-Bak BH3 peptide binding with IC50 of 1.5 μM and displaces Bax from Bcl-XL. Chelerythrine chloride induces apoptosis and autophagy. -
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AE 51310
0 ImagesCat. No.: HY-164428CAS No.: 433966-92-8 -
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C8 Dihydroceramide
0 ImagesC8 Dihydroceramide is a negative control of C8 Ceramide. C8-Ceramide (N-Octanoyl-D-erythro-sphingosine) is a cell-permeable analog of naturally occurring ceramides. C8-Ceramide has anti-proliferation properties and acts as a potent chemotherapeutic agent. C8-Ceramide stimulates dendritic cells to promote T cell responses upon virus infections. C8-Ceramide induces slight activation of protein kinase (PKC) in vitro. -
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- Pseudo RACK1
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JH-131e-153
0 ImagesCat. No.: HY-149489CAS No.: 742104-91-2JH-131e-153, a diacylglycerol (DAG)-lactone, is a small molecule activator of Munc13-1, targeting the C1 domain. The activation sequence of JH-131e-153 on Munc13-1 is WT>I590≈R592A≈W588A. The C1 domain of Munc13-1 and protein kinase C (PKC) are homologous in sequence and structure. The activation sequence of JH-131e-153 on Munc13-1 and PKC was PKCα>Munc13-1>PKCε. JH-131e-153 regulates neuronal processes through Munc13-1 and can be further used in the study of neurodegenerative diseases. -
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D-erythro-Sphingosine-13C2,d2
0 ImagesCat. No.: HY-101047S1CAS No.: 2692623-81-5Synonyms: Erythrosphingosine-13C2,d2; erythro-C18-Sphingosine-13C2,d2; trans-4-Sphingenine-13C2,d2D-erythro-Sphingosine-13C2,d2 is a deuterated labeled D-erythro-Sphingosine. D-erythro-Sphingosine (Erythrosphingosine) is a very potent activator of p32-kinase with an EC50 of 8 μM, and inhibits protein kinase C (PKC). D-erythro-Sphingosine (Erythrosphingosine) is also a PP2A activator. -
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Go 6983 (GMP)
0 ImagesCat. No.: HY-13689GCAS No.: 133053-19-7Go 6983 GMP is Go 6983 (HY-13689) produced by using GMP guidelines. GMP small molecules works appropriately as an auxiliary reagent for cell therapy manufacture. Go 6983 is a dual inhibitor targeting Suv39h1/2 (KMT1A/KMT1B) and PKC, as well as a transcriptional activator capable of inducing DNA hypomethylation. Go 6983 stimulates the transcription of Prdm14 by reducing Suv39h1/2 protein levels, decreasing histone modifications in the Prdm14 promoter region, and increasing the recruitment of RNA polymerase II. Go 6983 induces genome-wide DNA hypomethylation by inhibiting de novo methyltransferase expression and increasing Tet1/Tet2 levels, thereby promoting self-renewal and pluripotency maintenance of stem cells. Meanwhile, Go 6983 can block PKC-mediated signaling pathways to reduce the expression of EMT-related genes and eliminate the upregulation of antioxidant genes downstream of NRF2. Go 6983 is mainly used in mechanism studies related to myocardial ischemia/reperfusion injury. -
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MPSD
0 ImagesCat. No.: HY-P10471CAS No.: 134248-85-4Synonyms: MARCKS-EDMPSD (MARCKS-ED) is a 25-amino acid peptide based on the effector domain sequence of the intracellular membrane protein myristoylated alanine-rich C-kinase substrate (MARCKS). MPSD can sense membrane curvature and recognize phosphatidylserine. MPSD can be utilized as biological probe to study membrane shape and lipid composition. -
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PKCiota-IN-1
0 ImagesCat. No.: HY-122857CAS No.: 2230052-97-6PKCiota-IN-1 (compound 51) is a potent PKCiota (PKC-ι) inhibitor with an IC50 of 2.7 nM. PKCiota-IN-1 also inhibits PKC-α and PKC-ε with IC50s of 45 nM and 450 nM, respectively. -
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CIDD-0072424
0 ImagesCat. No.: HY-158051CAS No.: 1620195-03-0CIDD-0072424 selectively inhibits Protein Kinase C-epsilon (PKCε) (Ki=54 nM). CIDD-0072424 reduces ethanol consumption and preference in a dose-dependent manner. -
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KRAKAKTTKKR
0 ImagesCat. No.: HY-P2582CAS No.: 118675-77-7KRAKAKTTKKR is a protein kinase C substrate. -
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HNS-32
0 ImagesCat. No.: HY-117135CAS No.: 186086-10-2HNS-32 is a compound with antiarrhythmic and vasodilatory effects in canine hearts, showing superior protective effects against ischemic and reperfusion arrhythmias compared to an equivalent dose of Mexiletine hydrochloride (HY-A0093). Furthermore, HNS-32 exhibits significant negative chronotropic effects on mammalian ventricular myocardium, indicating its potential application value in the study of acute coronary syndrome. -
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PKCd (8-17)
0 ImagesCat. No.: HY-P5452CAS No.: 379711-25-8PKCd (8-17) is a biological active peptide. (This peptide is derived from the V1 domain of protein kinase C (PKC)d. It inhibits phorbol 12-myristate 13-acetate (PMA)-induced PKCd translocation and activation. Inhibition of PKCd reduces ischemia damage in cardiac and cerebral cells, induces proliferation of fibroblasts, and inhibits graft coronary artery disease in mice.) -
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TAT-SAMβA
0 ImagesCat. No.: HY-P5891TAT-SAMβA is the peptide consist of RNAENFDRF (SAMβA; HY-P3429) conjugated to the cell penetrating TAT protein-derived peptide TAT47–57. TAT-SAMβA is a selective antagonist of Mfn1-βIIPKC association. TAT-SAMβA protects mouse embryonic fibroblast cells (MEFs) against oxidative stress-induced cytotoxicity. -
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Prkch Rat Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS11133Prkch Rat Pre-designed siRNA Set A contains three designed siRNAs for Prkch gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
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CMPD101 hydrochloride
0 ImagesCat. No.: HY-103045ACAS No.: 1941168-71-3CMPD101 hydrochloride is a novel membrane-permeable, small-molecule inhibitor of both GRK2 and GRK3 with IC50s of 18 nM and 5.4 nM, respectively. CMPD101 hydrochloride also inhibits Rho-associated kinase 2 (ROCK-2) and PKCα (IC50s =1.4 μM and 8.1 μM, respectively). -
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Phosphate acceptor peptide
0 ImagesCat. No.: HY-P3770CAS No.: 93511-94-5 -
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- [Ala107]MBP(104-118) TFA
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.