Succinyl-L-alanyl-L-alanine p-nitroanilide

• Description:

  Succinyl-L-alanyl-L-alanine p-nitroanilide Catalog number: MDP0155 CAS Number: 191338-86-0 Sequence: Succinyl-L-alanyl-L-alanine p-nitroanilide Amount: 20 mg Molecular Weight: 380 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: Erban T, Hubert J. Comparative analyses of proteolytic activities in seven species of synanthropic acaridid mites Arch Insect Biochem Physiol. 2010 Nov;75(3):187-206. 2: Ueki H, Furuta K, Funakoshi T, Matsunami Y, Kubota Y. Insulin-like activity of proteases. V. Stimulation of cyclic adenosine 3',5'-monophosphate phosphodiesterase by an N-succinyl-L-alanyl-L-alanyl-L-alanine p-nitroanilide-hydrolyzing protease Chem Pharm Bull (Tokyo). 1982 Mar;30(3):1054-8. 3: Levine EA, Senior RM, Butler JV. The elastase activity of alveolar macrophages: measurements using synthetic substrates and elastin Am Rev Respir Dis. 1976 Jan;113(1):25-30. 4: Ohlsson BG, Weström BR, Karlsson BW. Enzymoblotting: a method for localizing proteinases and their zymogens using para-nitroanilide substrates after agarose gel electrophoresis and transfer to nitrocellulose Anal Biochem. 1986 Feb 1;152(2):239-44. 5: Makimoto S, Taniguchi Y. Effect of pressure on the pre-steady-state kinetics of the hydrolysis of anilide substrates catalyzed by alpha-chymotrypsin Biochim Biophys Acta. 1987 Aug 21;914(3):304-7. 6: Saklatvala J. Hydrolysis of the elastase substrate succinyltrialanine nitroanilide by a metal-dependent enzyme in rheumatoid synovial fluid J Clin Invest. 1977 May;59(5):794-801. 7: Nascimento TP, Sales AE, Porto TS, Costa RMPB, Breydo L, Uversky VN, Porto ALF, Converti A. Purification, biochemical, and structural characterization of a novel fibrinolytic enzyme from Mucor subtilissimus UCP 1262 Bioprocess Biosyst Eng. 2017 Aug;40(8):1209-1219. 8: O'Neill S, Prichard JS. Elastolytic activity of alveolar macrophages in chronic bronchitis: comparison of current and former smokers Thorax. 1983 May;38(5):356-9. 9: Matsuda K, Mizuguchi K, Nishioka T, Kato H, Go N, Oda J. Crystal structure of glutathione synthetase at optimal pH: domain architecture and structural similarity with other proteins Protein Eng. 1996 Dec;9(12):1083-92. 10: Connolly L, Fodey TL, Crooks SR, Delahaut P, Elliott CT. The production and characterisation of dinitrocarbanilide antibodies raised using antigen mimics J Immunol Methods. 2002 Jun 1;264(1-2):45-51.
  Products Related to Succinyl-L-alanyl-L-alanine p-nitroanilide can be found at Peptides

• Short Description:

  Catalog Number: MDP0155 (20 mg) Succinyl-L-alanyl-L-alanine p-nitroanilide is a high quality Succinyl-L-alanyl-L-alanine 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.

• Weight:

  0.15

• Length:

  2

• Width:

  0.5

• Height :

  0.5