Suc-Ala-Ala-Pro-Phe-AMC

Suc-Ala-Ala-Pro-Phe-AMC

Product Number: 4012873

CAS Number: 88467-45-2

CHF 337.10 – CHF 1,349.30

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Product Description

The peptidylprolyl isomerase substrate Suc-AAPF-AMC is also hydrolyzed by carboxypeptidase Y, cathepsin G, and chymotrypsin. Suc-AAPF-AMC has also been used to analyze the chymotrypsin-like activity of trypsins.

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VIP/PACAP Peptides
Urotensin II: a somatostatin-like peptide in the caudal neurosecretory system of fishes.

D.Pearson et al., Proc. Natl. Acad. Sci. USA, 77, 5021 (1980)

A peptidyl-prolyl cis/trans-isomerase (cyclophilin G) in regulated secretory granules.

Y.Takaki et al., J. Biol. Chem., 272, 28615 (1997)

Interaction of alpha-chymotrypsin with dimyristoyl phosphatidylcholine vesicles.

G.Oshima, J. Biochem. (Tokyo), 95, 1131 (1984)

Stimulation by phospholipid vesicles of proteolysis of egg white lysozyme by chymotrypsin.

G.Oshima, J. Biochem. (Tokyo), 94, 1615 (1983)

Escherichia coli cyclophilin B binds a highly distorted form of trans-prolyl peptide isomer.

M.Konno et al., Eur. J. Biochem., 271, 3794 (2004)

Biochemical characterization of the prolyl 3-hydroxylase 1.cartilage-associated protein.cyclophilin B complex.

Y.Ishikawa et al., J. Biol. Chem., 284, 17641 (2009)

Selective alteration of substrate specificity by replacement of aspartic acid-189 with lysine in the binding pocket of trypsin.

L.Graf et al., Biochemistry, 26, 2616 (1987)

Selective alteration of substrate specificity by replacement of aspartic acid-189 with lysine in the binding pocket of trypsin.

L.Graf et al., Biochemistry, 26, 2616 (1987)

Design of protease-resistant myelin basic protein-derived peptides by cleavage site directed amino acid substitutions.

T.Burster et al., Biochem. Pharmacol., 74, 1514 (2007)

Molecular weight: 661.71

Sum Formula: C₃₄H₃₉N₅O₉

Storage Temperature: < -15°C

One Letter code: Suc-AAPF-AMC

Source: Synthetic

Old Product Number: I-1465

Substrates
Chymotrypsin
Carboxypeptidase C
Peptidylprolyl Isomerase
Cathepsin G

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