Amikacin Sulfate (1:1.8), AST grade

Amikacin Sulfate (1:1.8), AST grade

Catalog Number:
M001341784TOK
Mfr. No.:
TOK-A225-1G
Price:
$220
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      • Overview
        • Please contact us at for specific academic pricing.

          Background

          Amikacin Sulfate binds to the 30S ribosomal subunit (specifically the 16S rRNA and S12 protein) resulting in interference with the translational initiation complex and mRNA misreading, which leads to a faulty or nonexistent protein.

      • Properties
        • CAS Number
          39831-55-5
          Molecular Formula
          C22H43N5O13*1.8H2SO4
          Other Properties
          Source: Semi-synthetic
          Storage
          2-8°C

          * For research use only

      • Applications
        • Application Description
          Microbiology Applications: Amikacin Sulfate is commonly used in clinical in vitro microbiological antimicrobial susceptibility tests (panels, discs, and MIC strips) against Gram-negative microbial isolates. Medical microbiologists use this information to recommend antibiotic treatment options. Samples of microbes grown in presence of a 30 µg Amikacin disc with a zone of inhibition of <14 mm in diameter are considered resistant. Intermediate resistance zones of inhibition are typically 15 mm-16 mm in diameter. Representative MIC values include:
          Pseudomonas aeruginosa 0.25 µg/mL -512 µg/mLSerratia marcescens ≤0.25 µg/mL - >32 µg/mL
          Eukaryotic Cell Culture Applications: In vitro studies with Amikacin demonstrate lysosomal phospholipidosis, with the compound binding to the phospholipid bilayer.
          An LC–MS/MS assay was developed to quantify Amikacin in different biological matrices. This technology can facilitate future studies on improving Amikacin-associated nephrotoxicity. It would be useful for in vitro studies characterizing Amikacin uptake kinetics in renal cells, and in vivo pharmacokinetic studies (Chan et al, 2020).
          Contamination of cell cultures for virus isolation is problematic. Amikacin (and vancomycin ) were chosen to replace the penicillin and gentamicin used conventionally. This combination was not toxic to cell cultures remained stable in media for over six months. Virus isolation rate was maintained and contamination was reduced from 10% to 1.5%. This combination can be used for maintenance and transport media to control the emerging problem of viral culture contamination (Lo et el, 1996).

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