Glutaryl-L-alanyl-L-alanyl-L-prolyl-L-leucine p-nitroanilide

CAT:
952-MDP0173
Size:
20 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Glutaryl-L-alanyl-L-alanyl-L-prolyl-L-leucine p-nitroanilide - image 1
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Glutaryl-L-alanyl-L-alanyl-L-prolyl-L-leucine p-nitroanilide

  • Description:

    Glutaryl-L-alanyl-L-alanyl-L-prolyl-L-leucine p-nitroanilide Catalog number: MDP0173 CAS Number: N/A Sequence: Glutaryl-L-alanyl-L-alanyl-L-prolyl-L-leucine p-nitroanilide Amount: 20 mg Molecular Weight: 604.4 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: Abuin E, Lissi E, Duarte R. Kinetics of N-glutaryl-L-phenylalanine p-nitroanilide hydrolysis catalyzed by alpha-chymotrypsin in aqueous solutions of dodecyltrimethylammonium bromide J Colloid Interface Sci. 2005 Mar 15;283(2):539-43. 2: Abuin E, Lissi E, Calderón C. Kinetics of N-glutaryl-L-phenylalanine p-nitroanilide hydrolysis catalyzed by alpha-chymotrypsin in aqueous solutions of alkyltrimethylammonium bromides J Colloid Interface Sci. 2007 Apr 15;308(2):573-6. 3: Abuin E, Lissi E, Ahumada M, Calderón C. Effect of human serum albumin on the kinetics of N-glutaryl-L-phenylalanine p-nitroanilide hydrolysis catalyzed by α-chymotrypsin Protein J. 2011 Feb;30(2):143-7. 4: Hegazi FZ, Abo-Elnaga IG. Proteolytic activity of crude cell-free extract of Lactobacillus casei and Lactobacillus plantarum Nahrung. 1987;31(3):225-32. 5: Shibata Y, Fujimura S, Nakamura T. Purification and partial characterization of an elastolytic serine protease of Prevotella intermedia Appl Environ Microbiol. 1993 Jul;59(7):2107-11. 6: Twining SS, Brecher AS. Characterization of the interaction between chymotrypsin and heparin Can J Biochem. 1977 Feb;55(2):134-9. 7: Mao Q, Walde P. Substrate effects on the enzymatic activity of alpha-chymotrypsin in reverse micelles Biochem Biophys Res Commun. 1991 Aug 15;178(3):1105-12. 8: Brecher AS, Moehlman TA, Hann W. Utilization of chymotrypsin as a sole carbon and (or) nitrogen source by Escherichia coli Can J Microbiol. 1992 Apr;38(4):290-5. 9: Del Mar EG, Largman C, Brodrick JW, Fassett M, Geokas MC. Substrate specificity of human pancreatic elastase 2 Biochemistry. 1980 Feb 5;19(3):468-72. 10: Stevens ED, McLeese JM. Why bluefin tuna have warm tummies: temperature effect on trypsin and chymotrypsin Am J Physiol. 1984 Apr;246(4 Pt 2):R487-94.
    Products Related to Glutaryl-L-alanyl-L-alanyl-L-prolyl-L-leucine p-nitroanilide can be found at Peptides
  • Short Description:

    Catalog Number: MDP0173 (20 mg) Glutaryl-L-alanyl-L-alanyl-L-prolyl-L-leucine p-nitroanilide is a high quality Glutaryl-L-alanyl-L-alanyl-L-prolyl-L-leucine 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