851231-19-1

Basic information

• Product Name: (7-AMINO-4-METHYLCOUMARIN-3-YL)ACETYL-GLU-GLU-LYS-PRO-ILE-SER-PHE-PHE-ARG-LEU-GLY-LYS(BIOTINYL)-NH2
• Synonyms: (7-AMINO-4-METHYLCOUMARIN-3-YL)ACETYL-GLU-GLU-LYS-PRO-ILE-SER-PHE-PHE-ARG-LEU-GLY-LYS(BIOTINYL)-NH2;AMCA-GLU-GLU-LYS-PRO-ILE-SER-PHE-PHE-ARG-LEU-GLY-LYS(BIOTINYL)-NH2;(7-Amino-4-methylcoumarin-3-yl)acetyl-Glu-Glu-Lys-
• CAS NO: 851231-19-1
• Molecular Formula: C90H131N21O22S
• Molecular Weight: 1891.22
• Mol File: 851231-19-1.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (7-AMINO-4-METHYLCOUMARIN-3-YL)ACETYL-GLU-GLU-LYS-PRO-ILE-SER-PHE-PHE-ARG-LEU-GLY-LYS(BIOTINYL)-NH2(CAS DataBase Reference)
• NIST Chemistry Reference: (7-AMINO-4-METHYLCOUMARIN-3-YL)ACETYL-GLU-GLU-LYS-PRO-ILE-SER-PHE-PHE-ARG-LEU-GLY-LYS(BIOTINYL)-NH2(851231-19-1)
• EPA Substance Registry System: (7-AMINO-4-METHYLCOUMARIN-3-YL)ACETYL-GLU-GLU-LYS-PRO-ILE-SER-PHE-PHE-ARG-LEU-GLY-LYS(BIOTINYL)-NH2(851231-19-1)

Safety Data

• Hazardous Substances Data: 851231-19-1(Hazardous Substances Data)

Usage

Description

(7-AMINO-4-METHYLCOUMARIN-3-YL)ACETYL-GLU-GLU-LYS-PRO-ILE-SER-PHE-PHE-ARG-LEU-GLY-LYS(BIOTINYL)-NH2 is a complex peptide that incorporates a fluorescent coumarin group, an acetyl group, and a biotinylated lysine residue. This peptide is composed of various amino acids, including glutamine, lysine, proline, isoleucine, serine, phenylalanine, arginine, leucine, and glycine, with a biotinylated lysine at the terminal end. It is widely utilized in molecular biology and biochemistry research for probing biological processes and as a molecular tag for immunoassays and protein purification techniques. The 7-amino-4-methylcoumarin group endows the peptide with fluorescent properties, while the biotinylated lysine enables specific binding to streptavidin or avidin in affinity purification and detection assays.

Uses

Used in Molecular Biology Research:
(7-AMINO-4-METHYLCOUMARIN-3-YL)ACETYL-GLU-GLU-LYS-PRO-ILE-SER-PHE-PHE-ARG-LEU-GLY-LYS(BIOTINYL)-NH2 is used as a probe for studying various biological processes and interactions within the molecular biology field. The fluorescent properties of the coumarin group allow for easy tracking and visualization of the peptide in biological systems.
Used in Biochemistry Research:
In biochemistry, this peptide is employed as a molecular tag for immunoassays, which are essential for detecting and quantifying specific proteins or other molecules of interest. The biotinylated lysine residue facilitates specific binding to streptavidin or avidin, enhancing the sensitivity and specificity of these assays.
Used in Protein Purification Techniques:
(7-AMINO-4-METHYLCOUMARIN-3-YL)ACETYL-GLU-GLU-LYS-PRO-ILE-SER-PHE-PHE-ARG-LEU-GLY-LYS(BIOTINYL)-NH2 is used as an affinity tag for protein purification. The biotinylated lysine allows for specific binding to streptavidin or avidin, which can be immobilized on a solid support, enabling the purification of target proteins through affinity chromatography.
Used in Diagnostics and Detection Assays:
This peptide is utilized as a detection agent in various diagnostic assays, taking advantage of its fluorescent properties. The coumarin group allows for the detection of the peptide and any associated molecules through fluorescence-based techniques, which can be applied in the development of sensitive and specific diagnostic tools.
Used in Pharmaceutical Development:
(7-AMINO-4-METHYLCOUMARIN-3-YL)ACETYL-GLU-GLU-LYS-PRO-ILE-SER-PHE-PHE-ARG-LEU-GLY-LYS(BIOTINYL)-NH2 may also be used in the development of new pharmaceuticals, particularly in the design of targeted drug delivery systems. The peptide's properties can be exploited to create molecules that specifically bind to certain receptors or proteins, potentially enhancing the efficacy and selectivity of therapeutic agents.