|Related Categories||Cell Lysis and Protein Extraction Reagents, Chemical Modification Reagents, Native Protein Sample Preparation, Protein Modification, Protein Structural Analysis,|
|packaging||vial of 56 mg|
Alkylating reagent for cysteine residues in peptide sequencing. By virtue of reaction with cysteine, it is an irreversible inhibitor of enzymes with cysteine at the active site.1 It reacts much more slowly with histidine residues, but that activity is responsible for inhibition of ribonuclease.2
For use in 2-D protein electrophoresis. Eliminates artifacts of disulfide formation during electrophoresis for less streaking and better resolution.
Packaged in sealed ampules
Technology developed in partnership with Proteome Systems™
Proteome Systems is a trademark of Proteome Systems Ltd
Certificate of Analysis
Certificate of Origin
|Precautionary statements||P261-P280-P301 + P310-P342 + P311|
|Personal Protective Equipment||Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges|
|Hazard Codes (Europe)||T|
|Risk Statements (Europe)||25-42/43-53|
|Safety Statements (Europe)||22-36/37-45|
|RIDADR||UN 2811 6.1/PG 3|
Antiviral Activity of RhoA-Derived Peptides against Respiratory Syncytial Virus Is Dependent on Formation of Peptide Dimers. Budge, P.J., et al. Antimicrob. Agents Chemother. 47(11), 3470-3477, (2003)
Oviduct-specific glycoprotein and heparin modulate sperm–zona pellucida interaction during fertilization and contribute to the control of polyspermy. Coy, P., et al. Proc. Natl. Acad. Sci. U. S. A. 105(41), 15809-15814, (2008)
Aldrich MSDS 1, 1089:C / Corp MSDS 1 (1), 1990:B / FT-IR 2 (1), 1259:C / FT-IR 1 (1), 751:B / IR-Spectra (2), 389:B / IR-Spectra (3), 439:C / NMR-Reference 2 (1), 632:C / RegBook 1 (1), 879:D / Sax 6, 1617 / Sigma FT-IR 1 (2), 656:D / Structure Index 1, 134:B:5
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