Ca2+/Calmodulin Kinase II Inhibitor 281-309

Code: 208711-500UG D2-231

Biochem/physiol Actions

Cell permeable: no

Reversible: no

Product does not compete with ATP.

General description

A synthetic peptide ...


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Your Price
€204.56 EACH
Discontinued
€251.61 inc. VAT

Biochem/physiol Actions

Cell permeable: no

Reversible: no

Product does not compete with ATP.

General description

A synthetic peptide that contains the CaM-binding, inhibitory, and autophosphorylation domains of CaM kinase II. Can be phosphorylated at Thr286 by PKC. Useful as a calmodulin binding peptide. Inhibits CaM kinase II (IC50 = 80 nM) by blocking Ca2+/calmodulin activation and enzyme active site (IC50 = 2 µM).

A synthetic peptide containing the calmodulin binding site (290-309) and the autophosphorylation site (Thr286) of CaM kinase II. Can be phosphorylated at Thr286 by PKC. Useful as a calmodulin binding peptide. Inhibits CaM kinase II by blocking Ca2+/calmodulin activation (IC50 = 80 nM) and enzyme-active site (IC50 = 2 µM).

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Other Notes

Waxham, M.N., et al. 1993. Biochemistry32, 2923.Waxham, M.N., et al. 1993. Brain Res. 609, 1.Fukunaga, K., et al. 1990. J. Neurochem.54, 103.Colbran, R.J., et al. 1989. J. Biol. Chem. 264, 4800.Colbran, R.J., et al. 1988. J. Biol. Chem.263, 18145.

Packaging

Yes

500 µg in Plastic ampoule

Sequence

H-Met-His-Arg-Gln-Glu-Thr-Val-Asp-Cys-Leu-Lys-Lys-Phe-Asn-Ala-Arg-Arg-Lys-Leu-Lys-Gly-Ala-Ile-Leu-Thr-Thr-Met-Leu-Ala-OH

Warning

Toxicity: Standard Handling (A)

assay≥97% (HPLC)
formlyophilized solid
manufacturer/tradenameCalbiochem®
potency80 nM IC50
Quality Level100
shipped inambient
solubilitywater: 5 mg/mL
storage conditiondesiccated (hygroscopic), OK to freeze
storage temp.−20°C
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