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  • Search results for: 'research area apoptosis bcl 2 family'

Search results for: 'research area apoptosis bcl 2 family'

Items 1-10 of 16

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  1. 2-Deoxyuridine
    B7866 2-Deoxyuridine
    Summary: Studies of DNA synthesis and degradation mechanisms.
      ≥22.8 mg/mL
  2. Mitomycin C
    A4452 Mitomycin C
     3 Citation
    Summary: Inhibits DNA synthesis,antibiotic and antitumor agent
      insoluble in H2O; insoluble in EtOH; ≥16.7 mg/mL
  3. Viomycin
    A8645 Viomycin
    Summary: Antibiotic of tuberactinomycin family
      <66.14 mg/mL
  4. Mercaptopurine (6-MP)
    A2355 Mercaptopurine (6-MP)
    Summary: Purine synthesis inhibitor
      insoluble in EtOH; insoluble in H2O; ≥7.61 mg/mL
  5. Ifosfamide
    A2097 Ifosfamide
    Target: DNA Alkylating
    Summary: Cytostatic agent
      ≥13.05 mg/mL
  6. Adenine sulfate
    B1469 Adenine sulfate
    Summary: Sulfate salt form of adenine
      insoluble in EtOH; ≥66.9 mg/mL
  7. Thiostrepton
    B7336 Thiostrepton
    Target: FoxM1
    Summary: Antibiotic that inhibits bacterial protein synthesis
      insoluble in EtOH; insoluble in H2O; ≥14.4 mg/mL
  8. Puromycin dihydrochloride
    B7587 Puromycin dihydrochloride
    Summary: allows selection for cells expressing the resistance gene puromycin N-acetyl-transferase (PAC) and successful Cas9-induced knock-in with puromycin resistance gene.
      ≥27.2 mg/mL
  9. Gemcitabine
    A8437 Gemcitabine
     1 Citation
    Summary: inhibitor of DNA synthesis
      ≥11.75 mg/mL
  10. Cladribine
    A2187 Cladribine
    Target: Adenosine Deaminases
    Summary: Apoptosis inducer in CLL cells
      ≥41.67 mg/mL

Items 1-10 of 16

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