Histone H2A (Xenopus, recombinant)
Histone H2A (Xenopus, recombinant)
Histone H2A is a core histone that forms a dimer with histone H2B.{46631} Two histone H2A/H2B dimers form an octameric...
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From €108.00 €91.80
From €108.00 €91.80
Ceftazidime is a cephalosporin antibiotic.{58320} It is active against isolates of numerous Gram-positive and Gram-negative bacteria, including E. coli, K. pneumoniae, P. mirabilis, and S. pyogenes (MICs = 0.015-8 µg/ml for all). It binds to E. coli penicillin-binding protein 1a (PBP1a), -1b, -2, and -3 (IC50s = 0.9, 3.4, 240, and 0.06 µg/ml, respectively).{57920} Ceftazidime increases survival in mice infected with strains of S. aureus, E. coli, K. pneumoniae, Proteus, or Serratia (ED50s = 0.1-25 mg/kg for all).{58320} Formulations containing ceftazidime have been used in the treatment of bacterial infections.
Territorial Availability: Available through Bertin Technologies only in France
| Size | 1 g, 10 g, 5 g, 500 mg |
|---|---|
| Shipping | dry ice |
| CAS number | 78439-06-2 |
| Molecular formula | C22H22N6O7S2 • 5H2O |
| Smiles | O=C(C1NC(/C(C2=CSC(N)=N2)=NOC(C)(C)C(O)=O)=O)N3[C@]1([H])SCC(C[N+]4=CC=CC=C4)=C3C([O-])=O.O.O.O.O.O, O=C(C1NC(/C(C2=CSC(N)=N2)=NOC(C)(C)C(O)=O)=O)N3[C@]1([H])SCC(C[N+]4=CC=CC=C4)=C3C([O-])=O.O.O.O.O.O, O=C(C1NC(/C(C2=CSC(N)=N2)=NOC(C)(C)C(O)=O)=O)N3[C@]1([H])SCC(C[N+]4=CC=CC=C4)=C3C([O-])=O.O.O.O.O.O, O=C(C1NC(/C(C2=CSC(N)=N2)=NOC(C)(C)C(O)=O)=O)N3[C@]1([H])SCC(C[N+]4=CC=CC=C4)=C3C([O-])=O.O.O.O.O.O |
| Molecular weight | 636,7 |
| Custom code | 2933.49 |
| Formulation | A crystalline solid |
| Purity | ≥95% |
| UNSPSC code | 12352100 |
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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.
Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.
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