PKC
Protein kinase C
PKC Isoform Specific Products
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PKC
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PKCα
(48)
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PKCβ
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PKCγ
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PKCδ
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PKCε
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PKCη
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PKCζ
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PKCθ
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PKCμ
(4)
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PKC-ι ℩
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PKCι
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PKC Related Products (504)
Related Products (504)
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Antibodies (21)
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PKC Isoform Comparison
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Prkcb Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS11120Prkcb Mouse Pre-designed siRNA Set A contains three designed siRNAs for Prkcb gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.
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- [Ala107]MBP(104-118) acetate
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- Enzastaurin dihydrochloride
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Calphostin I
0 ImagesCat. No.: HY-N19701CAS No.: 124857-59-6Calphostin I is a selective protein kinase C (PKC) inhibitor with an IC50 of 0.14 μM in rats. Calphostin I interacts with the regulatory domain of PKC, and the aromatic groups at its C-14 and C-17 positions contribute to enhanced potency and selectivity, with no inhibition of cyclic adenosine monophosphate-dependent protein kinase (PKA) at high concentrations. Calphostin I can be used in research related to cervical cancer and breast cancer. -
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PS315
0 ImagesCat. No.: HY-124308CAS No.: 1221964-50-6PS315, a derivative of PS48 (HY-15967), is an allosteric PKC inhibitor by binding to the PIF-pocket of aPKC and inducing a displacement of the active site residue Lys111. PS315 inhibits the full-length and catalytic domain constructs of PKCζ (IC50=10 μM) and PKCη (IC50=30 μM). PS315 has anti-cancer activity. -
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PKCTheta-IN-1
0 ImagesCat. No.: HY-162234CAS No.: 2948289-20-9PKCTheta-IN-1 (Compound 19) is a selective macrocyclic PKCTheta inhibitor with IC50 value of 0.1 nM. -
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PKC-IN-7
0 ImagesCat. No.: HY-177283CAS No.: 611234-91-4 -
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6-Deoxyisojacareubin
0 ImagesCat. No.: HY-N8475CAS No.: 26486-92-0 -
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Prkce Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS11126Prkce Mouse Pre-designed siRNA Set A contains three designed siRNAs for Prkce gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.
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[Ala113]MBP(104-118)
0 ImagesCat. No.: HY-P1289CAS No.: 99026-78-5[Ala113]MBP(104-118) is an noncompetitive peptide inhibitors of protein kinase C (PKC), with IC50s ranging from 28-62 μM. -
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Staurosporine-Boc
0 ImagesCat. No.: HY-164041CAS No.: 120685-17-8Staurosporine-Boc, a natural product isolated from the actinomyces Streptomyces staurosporeus, is a potent non-selective inhibitor of protein kinase. Staurosporine-Boc inhibits a variety of protein kinases, including protein kinase C (PKC), tyrosine kinase, and serine/threonine kinase. Because of its broad inhibition profile, Staurosporine-Boc is widely used as a tool compound in biological research, especially when studying cell signaling pathways. -
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- (Rac)-Aurora A/PKC-IN-1
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PRKCE Human Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS11125PRKCE Human Pre-designed siRNA Set A contains three designed siRNAs for PRKCE gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Raxofelast
0 ImagesCat. No.: HY-120485CAS No.: 128232-14-4Synonyms: IRFI-016Raxofelast (IRFI-016) is an antioxidant agent in various models of ischemia-reperfusion injury. Raxofelast has antiproliferative activity in H2O2-stimulated rat aortic smooth muscle cells. Raxofelast attenuates the activation of mitogen-activating protein kinase (MAPK), ERK kinase 1, 2 (MEK1,2) and protein kinase C (PKC) without affecting Ras expression. -
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Phellodendrine chloride (Standard)
0 ImagesCat. No.: HY-N0735RCAS No.: 104112-82-5Phellodendrine chloride (Standard) is the analytical standard of Phellodendrine chloride (HY-N0735). Phellodendrine chloride is an orally active plant alkaloid. Phellodendrine chloride inhibits the proliferation of KRAS-mutated pancreatic cancer cells by suppressing macropinocytosis and glutamine metabolism, inducing ROS accumulation and mitochondrial apoptosis. Phellodendrine chloride promotes autophagy by activating the AMPK/mTOR pathway, alleviating intestinal damage in ulcerative colitis. Phellodendrine chloride can alleviate gouty arthritis by inhibiting the IL-6/STAT3 signaling pathway. Phellodendrine chloride suppresses allergic reactions by altering the conformation of MRGPRB3/MRGPRX2 protein, thereby inhibiting the activation of PKC and subsequent downstream MAPK and NF-κB signaling. Phellodendrine chloride inhibits the AKT/NF-κB pathway and down-regulates the expression of COX-2, thereby protecting zebrafish embryos from oxidative stress. Phellodendrine chloride has an anti-major depressive disorder (MDD) effect by down-regulating CHRM1, HTR1A, and the PI3K/Akt signaling pathway. -
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PRKCZ Human Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS11141PRKCZ Human Pre-designed siRNA Set A contains three designed siRNAs for PRKCZ gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Mitoxantrone-d8 dihydrochloride
0 ImagesCat. No.: HY-13502ASSynonyms: Mitozantrone-d8dihydrochloride; NSC 301739-d8 dihydrochlorideMitoxantrone-d8 dihydrochloride is deuterated labeled Mitoxantrone dihydrochloride (HY-13502A). Mitoxantrone dihydrochloride is a potent topoisomerase II inhibitor. Mitoxantrone dihydrochloride also inhibits protein kinase C (PKC) activity with an IC50 of 8.5 μM. Mitoxantrone dihydrochloride induces apoptosis of B-CLL (B-chronic lymphocytic leukaemia) cells. Mitoxantrone dihydrochloride shows antitumor activity. Mitoxantrone dihydrochloride also has anti-orthopoxvirus activity with EC50s of 0.25 μM and and 0.8 μM for cowpox and monkeypox, respectively. -
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TX-1918
0 ImagesCat. No.: HY-112393CAS No.: 503473-32-3TX-1918 is an inhibitor for eukaryotic elongation factor 2 kinase (eEF2-K) and Src kinase with IC50 of 0.44 and 4.4 μM, respectively. TX-1918 exhibits cytotoxicity in cell HepG2 and HCT116, with IC50 of 2.07 and 230 μM, respectively. TX-1918 inhibits the C-terminal domain of HIV-1 CA (CA CTD)(IC50 =3.81 μM), and inhibits the viral replication (IC50 =15.16 μM). -
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FIM-1
0 ImagesCat. No.: HY-D1493CAS No.: 220518-50-3 -
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Lyso-monosialoganglioside GM2 ammonium
0 ImagesCat. No.: HY-172546Purity: 98%Synonyms: LysoGM2 ammoniumLyso-monosialoganglioside GM2 (LysoGM2) ammonium is a lysosphingolipid and protein kinase C inhibitor (IC50: 50 μM). Lyso-monosialoganglioside GM2 ammonium can inhibit the binding of protein kinase C to Phorbol 12,13-dibutyrate (HY-18985). Lyso-monosialoganglioside GM2 ammonium is a specific biomarker for GM2 gangliosidosis. Lyso-monosialoganglioside GM2 ammonium can be used in the research of sphingolipidoses. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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