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product name Blasticidin S HCl


Description: Blasticidin S HCl is a nucleoside antibiotic isolated from Stretomyces girseochromogenes, and acts as a DNA and protein synthesis inhibitor, it is used to select transfected cells carrying bsr or BSD resistance genes. In mouse leukemia L5178Y cells, blasticidin S inhibited protein synthesis and caused the degradation of presumptive mRNA [1]. Also, blasticidin S inhibited ribonuclease P activity from Dictyostelium discoideum and inhibited tRNA maturation in a dose dependent way.

References: J Biochem. 1966 Dec;60(6):632-42; Biochim Biophys Acta. 1977 Mar 2;475(1):14-22.



Molecular Weight (MW)

458.9 
Formula

C17H27ClN8O5 
CAS No.

3513-03-9 
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: <1 mg/mL
Water: 91 mg/mL (198.3 mM)  
Ethanol: <1 mg/mL
Solubility (In vivo)

 
Synonyms

 

other peoduct :References PubMed ID::http://www.ncbi.nlm.nih.gov/pubmed/19411820

In Vitro

In vitro activity: Blasticidin S inhibits protein synthesis by acting on the step of peptide transfer from peptidyl-sRNA to incoming aminoacyl-sRNA. Blasticidin S also significantly inhibits DNA synthesis independent of their effect on protein synthesis. Blasticidin S kills the cells more rapidly than G418, which makes blasticidin S-resistance gene (bsr) a selectable marker for mammalian cells. Besides, Blasticidin S also efficiently binds Cu(II) ions and prevents DNA from metal-induced damage.


Kinase Assay:


Cell Assay

In Vivo  
Animal model  
Formulation & Dosage  
References J Biochem. 1966 Dec;60(6):632-42; Biochim Biophys Acta. 1977 Mar 2;475(1):14-22. 

MI-773

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Author: Sodium channel