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t-Butyloxycarbonyl-L-leucyl-L-seryl-L-threonyl-L-arginine p-nitroanilide

$695.00

Catalog Number: MDP0165 (5 mg)
t-Butyloxycarbonyl-L-leucyl-L-seryl-L-threonyl-L-arginine p-nitroanilide is a high quality t-Butyloxycarbonyl-L-leucyl-L-seryl-L-threonyl-L-arginine p-nitroanilide. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

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Description

t-Butyloxycarbonyl-L-leucyl-L-seryl-L-threonyl-L-arginine p-nitroanilide
Catalog number: MDP0165
CAS Number: 102129-66-8
Sequence: t-Butyloxycarbonyl-L-leucyl-L-seryl-L-threonyl-L-arginine p-nitroanilide
Amount: 5 mg
Molecular Weight: 695.6 g/mol
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: -20 °C
WARNING: For in vitro Research Use Only. NOT for use on humans or animals.
Grade: Biotechnology grade. All products are highly pure.

References:
1: Hayakawa T, Naruse S, Kitagawa M, Kondo T. [Elastase] Nihon Rinsho. 1995 May;53(5):1192-7.
2: Sharma SK, Castellino FJ. The chemical synthesis of the chromogenic substrates, H-D-Val-L-Leu-L-Lys-p-nitroanilide (S2251) and H-D-Ile-L-Pro-L-ARG-p-nitroanilide (S2288) Thromb Res. 1990 Jan 1;57(1):127-38.
3: Filippova IYu, Lysogorskaya EN, Oksenoit ES, Rudenskaya GN, Stepanov VM. L-Pyroglutamyl-L-phenylalanyl-L-leucine-p-nitroanilide–a chromogenic substrate for thiol proteinase assay Anal Biochem. 1984 Dec;143(2):293-7.
4: Kramps JA, van Twisk C, van der Linden AC. L-Pyroglutamyl-L-prolyl-L-valine-p-nitroanilide, a highly specific substrate for granulocyte elastase Scand J Clin Lab Invest. 1983 Sep;43(5):427-32.
5: Babbedge RC, Wallace P, Gaffen ZA, Hart SL, Moore PK. L-NG-nitro arginine p-nitroanilide (L-NAPNA) is anti-nociceptive in the mouse Neuroreport. 1993 Mar;4(3):307-10.
6: Held C, Stolzke T, Knierbein M, Jaworek MW, Luong TQ, Winter R, Sadowski G. Cosolvent and pressure effects on enzyme-catalysed hydrolysis reactions Biophys Chem. 2019 Sep;252:106209.
7: Doi M, Shioi Y, Sasa T. Purification and characterization of benzoyl-L-arginine p-nitroanilide hydrolase from etiolated leaves of Zea mays Arch Biochem Biophys. 1986 Nov 1;250(2):358-63.
8: Jacquot-Armand Y, Krebs G. Mise en evidence de la formation d’un complexe ternaire entre trypsine, alpha(2)-macroglobuline et inhibiteur basique de pancreas FEBS Lett. 1969 Jul;4(1):21-24.
9: Tsunematsu H, Imamura T, Makisumi S. Kinetics of hydrolysis of Na-benzoyl-p-guanidino-L-phenylalanine p-nitroanilide by trypsin J Biochem. 1983 Jul;94(1):123-8.
10: Gofshtein-Gandman LV, Keynan A, Milner Y. Bacteria of the genus Bacillus have a hydrolase stereospecific to the D isomer of benzoyl-arginine-p-nitroanilide J Bacteriol. 1988 Dec;170(12):5895-900.

Products Related to t-Butyloxycarbonyl-L-leucyl-L-seryl-L-threonyl-L-arginine p-nitroanilide can be found at Peptides

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