Spectinomycin dihydrochloride pentahydrate, Cell Culture Grade
Spectinomycin dihydrochloride pentahydrate, Cell Culture Grade
Spectinomycin dihydrochloride pentahydrate, Cell Culture Grade
Spectinomycin dihydrochloride pentahydrate, Cell Culture Grade
Thermo Scientific Chemicals

Spectinomycin dihydrochloride pentahydrate, Cell Culture Grade

Spectinomycin dihydrochloride pentahydrate, CAS # 22189-32-8, is the hydrochloride salt form of spectinomycin, an aminocyclitol compound showing antibacterial and antimicrobial activities. | CAS: 22189-32-8 | C14H36Cl2N2O12 | 495.34 g/mol
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Catalog NumberQuantity
ALFJ61820.1425 g
Catalog number ALFJ61820.14
Price (MYR)
2,119.00
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Quantity:
25 g
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Price (MYR)
2,119.00
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Specifications
Chemical Name or MaterialSpectinomycin dihydrochloride pentahydrate
TypeSpectinomycin Dihydrochloride Pentahydrate
Physical FormPowder
CAS22189-32-8
Health Hazard 1H315-H319-H335
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This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Suitable for battery materials development.

General Description

  • Spectinomycin dihydrochloride pentahydrate is derived from Streptomyces spectabilis and presents antibacterial and antimicrobial activities
  • Spectinomycin hydrochloride is a compound that inhibits the 30S ribosomal subunit of bacteria and interrupts protein synthesis and peptide elongation, leading to bacterial cell death

Application

  • Spectinomycin dihydrochloride pentahydrate is a compound that is active against gram-negative bacteria
  • In the laboratory, this compound is used in cell culture applications
  • It prevents contamination and can be used to select for resistant bacteria and plant cells containing the marker gene Spcr
  • It has been used to study respiratory tract infections caused by Pasteurella multocida and Mannheimia haemolytica
  • In genetic approaches, this compound can be used to amplify the plasmid copy number
RUO – Research Use Only

General References:

  1. Korte, H. L.; Saini, A.; Trotter, V. V.; Butland, G. P.; Arkin, A. P.; Wall, J. D. Independence of nitrate and nitrite inhibition of Desulfovibrio vulgaris Hildenborough and use of nitrite as a substrate for growth. Environ. Sci. Technol. 2015, 49 (2), 924-931.
  2. Pernil, R.; Picossi, S.; Herrero, A.; Flores, E.; Mariscal, V. Amino Acid Transporters and Release of Hydrophobic Amino Acids in the Heterocyst-Forming Cyanobacterium Anabaena sp. Strain PCC 7120. Life 2015, 5 (2), 1282-1300.