Catalog Number: MDP0089 (10 mg)
Benzoylglycyl-L-histidyl-L-leucine is a high quality Benzoylglycyl-L-histidyl-L-leucine. 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.
Live enquiry about this product via Text/SMS: 1-858-900-3210.
Catalog number: MDP0089
CAS Number: 2419-99-0
Amount: 10 mg
Molecular Weight: 429.2 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.
1: Moore GJ, Benoiton NL. Effect of the basic amino-acid side chain length and the penultimate residue on the hydrolysis of benzoldipeptides by carboxypeptidase B Can J Biochem. 1978 May;56(5):315-8.
2: Itakura K, Uchida K. Reaction of N(alpha)-hippuryllysine with 2-hydroxyheptanal: a model for lysine-directed protein modifications by lipid peroxidation Chem Phys Lipids. 2003 Jul;124(2):81-8.
3: Koide A, Yoshizawa M, Kurachi K. Crystallization and properties of carboxypeptidase A gamma from porcine pancreas Eur J Biochem. 1981 Jul;117(2):383-8.
4: Globisch M, Schindler M, Kreßler J, Henle T. Studies on the reaction of trans-2-heptenal with peanut proteins J Agric Food Chem. 2014 Aug 20;62(33):8500-7.
5: Houard X, Williams TA, Michaud A, Dani P, Isaac RE, Shirras AD, Coates D, Corvol P. The Drosophila melanogaster-related angiotensin-I-converting enzymes Acer and Ance–distinct enzymic characteristics and alternative expression during pupal development Eur J Biochem. 1998 Nov 1;257(3):599-606.
6: Sebastian JF, Hinks RS, Reuland RV. Kinetic studies of modifier effects on the carboxypeptidase A catalyzed hydrolyses of peptides Biochem Cell Biol. 1987 Aug;65(8):717-25.
7: Fukuda M, Shima H, Kunugi S. Kinetic study of carboxypeptidase P-catalyzed reaction. Pressure and temperature dependence of kinetic parameters J Biochem. 1985 Aug;98(2):517-25.
8: Turner AJ, Hryszko J, Hooper NM, Dowdall MJ. Purification and characterization of a peptidyl dipeptidase resembling angiotensin converting enzyme from the electric organ of Torpedo marmorata J Neurochem. 1987 Mar;48(3):910-6.
9: Carmel A, Yaron A. An intramolecularly quenched fluorescent tripeptide as a fluorogenic substrate of angiotensin-I-converting enzyme and of bacterial dipeptidyl carboxypeptidase Eur J Biochem. 1978 Jun 15;87(2):265-73.
10: Breslow R, Chin J, Hilvert D, Trainor G. Evidence for the general base mechanism in carboxypeptidase A-catalyzed reactions: partitioning studies on nucleophiles and H2(18)O kinetic isotope effects Proc Natl Acad Sci U S A. 1983 Jul;80(14):4585-9.
Products Related to Benzoylglycyl-L-histidyl-L-leucine can be found at Peptides
|Dimensions||8 × 8 × 8 in|
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