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Blasticidin S HCl |产品详情|进口橙子视频旧款采购网




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    Blasticidin S HCl
    品牌:AG Scientific
    货号:
    规格:25 mg
    货期:

    CAS:3513-03-9Formula:C17H26N8O5.HClMW:458.9Appearance:WhitePowderPurity:>98%

    商品详情 参考文献 相关资料

    Blasticidin S.H.cl is an aminoacylnucleoside antibiotic isolated from Streptomyces griseochromogenes. It shows high efficacy against both eukaryotic and prokaryotic cells. Aside from its antimicrobial properties, blasticidin has displayed antiviral, antitumor, and antifungal properties and has been used as a selection agent. It has been used to select for cells containing the blsbsr, or BSD resistance gene as well as HEK293-T cells and HEK-D5 cells. Additionally, blasticidin is effective in preventing cell culture contamination and studying protein synthesis.

    Blasticidin S.Hcl functions by inhibiting peptide bond formation at the ribosome. It blocks hydrolysis of peptidyl-tRNA due to the large ribosomal subunit's increased affinity for tRNA. Blasticidin S.Hcl has a longstanding application as a gene selection antibiotic and has a powerful new role in Genome editing utilizing the CRISPR/Cas9 system. 

     

    Additional Information

    Product #B-1247
    CAS #3513-03-9
    Chemical Name(2S,3S,6R)-3-[[(3S)-3-AMINO-5-[CARBAMIMIDOYL(METHYL)AMINO]PENTANOYL]AMINO]-6-(4-AMINO-2-OXOPYRIMIDIN-1-YL)-3,6-DIHYDRO-2H-PYRAN-2-CARBOXYLIC ACID HYDROCHLORIDE
    FormulaC17H26N8O5.HCl
    MW458.9
    AppearanceWhite Powder
    Purity>98%
    SolubilitySoluble in water. Clear and faint yellow solution at 5 mg/ml in water. Insoluble in organic solvents.
    Melting Point218.0-225.0 °C
    Storage TempStore desiccated at +4°C. Protect from moisture.
    UseAn antibiotic inhibiting protein synthesis

    Additional Information

    MDL NumberMFCD02091640
    ChemACXX1339381-2
    InChIInChI=1S/C17H26N8O5.ClH/c1-24(16(20)21)6-4-9(18)8-12(26)22-10-2-3-13(30-14(10)15(27)28)25-7-5-11(19)23-17(25)29;/h2-3,5,7,9-10,13-14H,4,6,8,18H2,1H3,(H3,20,21)(H,22,26)(H,27,28)(H2,19,23,29);1H
    SMILES[H]/N=C(N)/N(C)CCC(CC(=O)NC1C=CC(OC1C(=O)O)n2ccc(nc2=O)N)N.Cl
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