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P9200 Puromycin Dihydrochloride CAS: 58-58-2

Specifications
References
CAS Number
58-58-2
Grade
Molecular Biology Grade
Molecular Formula
C22H29N7O5•2HCl
Molecular Weight
544.44
EU Commodity Code
38220090
Shipping Temp
RT
Storage Temp
-20°C
(3’-[a-Amino-p-methoxyhydrocinnamamido]-3’deoxy-N,N-dimethyladenosine) dihydrochloride; Achromycin; Stillomycin; Stylomycin; Antibiotic CL 13900; Antibiotic 3123L; Antibiotic P638; Bacterenomycin; CL16,536; NSC 3055

Puromycin allows the selection of cells expressing the puromycin-N-acetyl-transferase (pac). The expression of pac gene confers puromycin resistance to transfected cells. Puromycin selection works for gram-positive bacteria and animal cells. Fungi and gram-negative bacteria are resistant due to low permeability of the antiboitic. Puromycin is an aminomucleoside antibiotic produced by Streptomyces alboniger. It is a powerful inhibitor of protein synthesis. It is a structural analog of the 3' end of animoacyl tRNA. When puromycin is added to an in vitro system containing all the necessary machinery for protein synthesis, protein synthesis stops and incomplete peptide chains are released from the ribosomes. Each such chain has puromycin covalently attached to one end.

Source
Streptomyces alboniger
Synonyms
(3’-[a-Amino-p-methoxyhydrocinnamamido]-3’deoxy-N,N-dimethyladenosine) dihydrochloride; Achromycin; Stillomycin; Stylomycin; Antibiotic CL 13900; Antibiotic 3123L; Antibiotic P638; Bacterenomycin; CL16,536; NSC 3055
CAS No
58-58-2
Molecular Formula
C22H29N7O5•2HCl
Molecular Weight
544.44
Appearance
White to off-white powder
Purity
≥98% (HPLC)
Solubility
Soulble in water
Melting Point
169-173°C
Working Concentration
1-10ug/ml in mammalian cell selection
Storage and Stability
Store at -20°C. Stable for 12 months after receipt.
Important Note
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Toxicity and Hazards
 All products should be handled by qualified personnel only, trained in laboratory procedures.
References
1. Nathans, D., Antibiotics, 1: 239 (1967). 2. Exp. Cell Res., 58: 401 (1969). 3. Mol. Biol., 79: 393 (1973). 4. Merck Index, 12: 8130 (1996).
USBio References
US Biological Application Reference: 1. Tappenden DM., et al. 2011. The aryl hydrocarbon receptor interacts with ATP5α1, a subunit of the ATP synthase complex, and modulates mitochondrial function. 254(3):299-310.
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