420311 Kanamycin Sulfate, Streptomyces kanamyceticus - CAS 25389-94-0 - Calbiochem

420311
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      Empirical FormulaCAS #
      C₁₈H₃₆N₄O₁₁ · H₂SO₄ 25389-94-0

      Precios y disponibilidad

      Número de referenciaDisponiblidad Embalaje Cant./Env. Precio Cantidad
      US1420311-25GM
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          Ampolla de plást. 25 gm
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          US1420311-5GM
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              Description
              OverviewContains more than 98% kanamycin A. An aminoglycoside antibiotic effective against Gram-positive and Gram-negative organisms. Inhibitor of protein biosynthesis that acts on the 30S ribosome, causing misreading of the genetic code. May cause renal damage and ototoxicity.
              Potency: ≥750 µg/mg
              Catalogue Number420311
              Brand Family Calbiochem®
              SynonymsKamycin
              References
              ReferencesLech, K., and Brent, R. 1995. in Current Protocols in Mol. Biol. Vol. 1 (Ausubel, F.M., et al., eds.) John Wiley & Sons, New York.
              Kahn, R.W., et al. 1993. Proc. Natl. Acad. Sci. USA 90, 9295.
              Cardon, G.H., et al. 1993. Plant J. 3, 773.
              Maniatis, T., et al. 1989. In Molecular Cloning, A Laboratory Manual, Second Edition. Cold Spring Harbor, New York. p.1.6, A.6.
              Korzybyski, T., et al. 1978. In Antibiotics, Origin, Nature, and Properties 1, 690.
              Stiffler, P.W., et al. 1974. Antimicrob. Agents Chemother. 6, 516.
              Umezawa, S., et al. 1968. J. Antibiot. 21, 367.
              Product Information
              CAS number25389-94-0
              FormWhite to off-white solid
              Hill FormulaC₁₈H₃₆N₄O₁₁ · H₂SO₄
              Chemical formulaC₁₈H₃₆N₄O₁₁ · H₂SO₄
              Structure formula ImageStructure formula Image
              Applications
              Biological Information
              Primary Targetprotein biosynthesis
              Physicochemical Information
              Dimensions
              Materials Information
              Toxicological Information
              Safety Information according to GHS
              RTECSNZ3225030
              Safety Information
              Product Usage Statements
              Storage and Shipping Information
              Ship Code Ambient Temperature Only
              Storage +15°C to +30°C
              Do not freeze Ok to freeze
              Special InstructionsFollowing reconstitution, sterilize by filtration through a 0.22 µm pore-size filter, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.
              Packaging Information
              Transport Information
              Supplemental Information
              Specifications

              Documentation

              Ficha datos de seguridad (MSDS)

              Título

              Ficha técnica de seguridad del material (MSDS) 

              Certificados de análisis

              CargoNúmero de lote
              420311

              Referencias bibliográficas

              Visión general referencias
              Lech, K., and Brent, R. 1995. in Current Protocols in Mol. Biol. Vol. 1 (Ausubel, F.M., et al., eds.) John Wiley & Sons, New York.
              Kahn, R.W., et al. 1993. Proc. Natl. Acad. Sci. USA 90, 9295.
              Cardon, G.H., et al. 1993. Plant J. 3, 773.
              Maniatis, T., et al. 1989. In Molecular Cloning, A Laboratory Manual, Second Edition. Cold Spring Harbor, New York. p.1.6, A.6.
              Korzybyski, T., et al. 1978. In Antibiotics, Origin, Nature, and Properties 1, 690.
              Stiffler, P.W., et al. 1974. Antimicrob. Agents Chemother. 6, 516.
              Umezawa, S., et al. 1968. J. Antibiot. 21, 367.

              Folleto

              Cargo
              Antibiotics Profiler
              Bulk Product Guide
              Drugs for Selection of Genetic Markers Technical Bulletin
              Overnight Express Autoinduction Systems

              Citas

              Título
            • Thomas S. Lendvay, et al. (2007) Compensatory paracrine mechanisms that define the urothelial response to injury in partial bladder outlet obstruction. American Journal of Physiology: Renal 293, F1147-F1156.
            • Ficha técnica

              Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

              Revision24-September-2010 JSW
              SynonymsKamycin
              DescriptionContains more than 98% kanamycin A. An aminoglycoside antibiotic affective against gram-positive and gram-negative organisms. Inhibitor of protein biosynthesis that acts on the 70S ribosome, causing misreading of the genetic code. May cause renal damage and ototoxicity.
              FormWhite to off-white solid
              CAS number25389-94-0
              RTECSNZ3225030
              Chemical formulaC₁₈H₃₆N₄O₁₁ · H₂SO₄
              Structure formulaStructure formula
              SolubilityH₂O (10 mg/ml)
              Storage +15°C to +30°C
              Do Not Freeze Ok to freeze
              Special InstructionsFollowing reconstitution, sterilize by filtration through a 0.22 µm pore-size filter, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.
              Merck USA index14, 5281
              ReferencesLech, K., and Brent, R. 1995. in Current Protocols in Mol. Biol. Vol. 1 (Ausubel, F.M., et al., eds.) John Wiley & Sons, New York.
              Kahn, R.W., et al. 1993. Proc. Natl. Acad. Sci. USA 90, 9295.
              Cardon, G.H., et al. 1993. Plant J. 3, 773.
              Maniatis, T., et al. 1989. In Molecular Cloning, A Laboratory Manual, Second Edition. Cold Spring Harbor, New York. p.1.6, A.6.
              Korzybyski, T., et al. 1978. In Antibiotics, Origin, Nature, and Properties 1, 690.
              Stiffler, P.W., et al. 1974. Antimicrob. Agents Chemother. 6, 516.
              Umezawa, S., et al. 1968. J. Antibiot. 21, 367.
              Citation
            • Thomas S. Lendvay, et al. (2007) Compensatory paracrine mechanisms that define the urothelial response to injury in partial bladder outlet obstruction. American Journal of Physiology: Renal 293, F1147-F1156.
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              Categorías

              Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Other Inhibitors of Biological Interest > Protein Synthesis Inhibitors
              Life Science Research > Inhibitors and Biochemicals > Biochemicals > Antibiotics > Antimicrobial Agents
              Life Science Research > Cell Culture and Systems > Antibiotics & Selection Agents