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Overview
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Vancomycin Hydrochloride, USP is a glycopeptide antibiotic derived from Streptomyces orientalis that was discovered in 1953 from a soil sample found in Borneo. It is effective against Gram-positive bacteria such as Staphylococcus aureus, including MRSA. Vancomycin HCl is commonly used in selective media for isolation of Gram-negative bacteria as well as studies of nanoparticle transport and antibiotic resistance.
Vancomycin HCl acts as a bacterial cell wall synthesis inhibitor by preventing the transfer and addition of NAM/NAG-peptides that make up the peptidoglycan cell wall structure.
Vancomycin HCl has low cell toxicity in plant cells and has been used in conjunction with Cefotaxime or Carbenicillin to stop the growth of Agrobacterium in plant cell culture and transformation.
Vancomycin Hydrochloride, USP conforms to United States Pharmacopoeia specifications.Please contact us at for specific academic pricing.
Background
Vancomycin HCl prevents cell wall synthesis by two separate mechanisms. One mechanism prevents N-acetylmuramic acid (NAM) and N-acetylglucosamine (NAG) peptides from linking together forming the peptidoglycan backbone through the incorporation of the Vancomycin HCl molecule to the D-alanyl-D-alanine terminal. The second mechanism prevents crosslinking between amino acid residues in the peptidoglycan chain altering bacterial cell membrane permeability as well as RNA synthesis.
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Overview
Vancomycin Hydrochloride, USP
Vancomycin Hydrochloride, USP
Catalog Number:
PB01342474TOK
Mfr. No.:
TOK-V001
Price:
$211
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