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  JNK Inhibitor III, Cell-Permeable
Cat. No. 420130  
All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » c-Jun N-Terminal Kinase (JNK/SAP Kinase)

Ac-YGRKKRRQRRR-gaba-ILKQSMTLNLADPVGSLKPHLRAKN-NH2
HIV-TAT47-57-gaba-c-Jund33-57
SAPK Inhibitor III

Lyophilized white solid. Supplied as a trifluoroacetate salt. PROTECT FROM LIGHT. HYGROSCOPIC. PACKAGED UNDER INERT GAS. A cell-permeable 37-mer peptide constructed by fusing human c-Jun d domain (amino acids 33-57) sequence with that of HIV-TAT protein transduction domain (amino acids 47-57) via a g-aminobutyric acid (GABA) spacer. Shown to specifically disrupt c-Jun/JNK complex formation and the subsequent phosphorylation and activation of c-Jun by JNK both in vitro and in intact cells. Since its mode of inhibition is different than that of JNK Inhibitor II (SP600125; Cat. No. 420119), these two inhibitors can complement each other in JNK signaling pathway studies. Purity: ≥95% by HPLC.

Ac-Tyr-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-gaba-Ile-Leu-Lys-Gln-Ser-Met-Thr-Leu-Asn-Leu-Ala-Asp-Pro-Val-Gly-Ser-Leu-Lys-Pro-His-Leu-Arg-Ala-Lys-Asn-NH2

Ref.: Holzberg, D., et al. 2003. J. Biol. Chem. 278, 40213.

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SolubilityMolecular FormulaMol. Wt.
DMSO C191H336N70O484413.3 

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420130: JNK Inhibitor III, Cell-Permeable - English
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Related Categories:
All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » c-Jun N-Terminal Kinase (JNK/SAP Kinase)