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C655639-1mlCCT244747 is a potent, orally bioavailable and highly selective CHK1 inhibitor, with an IC 50 of 7.7 nM: CCT244747 also abrogates G2 checkpoint with an IC 50 of 29 nM.In VitroCCT244747 poorly inhibits CHK2 (IC 50 >:10 μM) and CDK1 (IC 50 >:10
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C412010-100μgCemiplimab is a monoclonal IgG4 antibody with high affinity for programmed death receptor-1 (PD-1) that blocks PD-1/PD-L1 mediated T cell inhibition. It is commonly used in squamous cell skin cancer research.Purity>:95% (SDS-PAGE&:SEC)Endotoxin
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C412010-10mgCemiplimab is a monoclonal IgG4 antibody with high affinity for programmed death receptor-1 (PD-1) that blocks PD-1/PD-L1 mediated T cell inhibition. It is commonly used in squamous cell skin cancer research.Purity>:95% (SDS-PAGE&:SEC)Endotoxin
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C412010-1mgCemiplimab is a monoclonal IgG4 antibody with high affinity for programmed death receptor-1 (PD-1) that blocks PD-1/PD-L1 mediated T cell inhibition. It is commonly used in squamous cell skin cancer research.Purity>:95% (SDS-PAGE&:SEC)Endotoxin
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C412010-5mgCemiplimab is a monoclonal IgG4 antibody with high affinity for programmed death receptor-1 (PD-1) that blocks PD-1/PD-L1 mediated T cell inhibition. It is commonly used in squamous cell skin cancer research.Purity>:95% (SDS-PAGE&:SEC)Endotoxin
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D412005-100μgDurvalumab is an humanized anti-PD-L1 monoclonal antibody, completely blocks the binding of PD-L1 to both PD-1 and CD80, with IC50s of 0.1 and 0.04 nM, respectively.Purity>:95% (SDS-PAGE&:SEC)Endotoxin Level<:0.01EU/μg.
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D412005-10mgDurvalumab is an humanized anti-PD-L1 monoclonal antibody, completely blocks the binding of PD-L1 to both PD-1 and CD80, with IC50s of 0.1 and 0.04 nM, respectively.Purity>:95% (SDS-PAGE&:SEC)Endotoxin Level<:0.01EU/μg.
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D412005-1mgDurvalumab is an humanized anti-PD-L1 monoclonal antibody, completely blocks the binding of PD-L1 to both PD-1 and CD80, with IC50s of 0.1 and 0.04 nM, respectively.Purity>:95% (SDS-PAGE&:SEC)Endotoxin Level<:0.01EU/μg.
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D412005-5mgDurvalumab is an humanized anti-PD-L1 monoclonal antibody, completely blocks the binding of PD-L1 to both PD-1 and CD80, with IC50s of 0.1 and 0.04 nM, respectively.Purity>:95% (SDS-PAGE&:SEC)Endotoxin Level<:0.01EU/μg.
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G651939-100mgGDC-0425 (RG-7602) is an orally available, highly selective small molecule ChK1 inhibitor. GDC-0425 can be used for the research of various malignanciesIn VitroMEK inhibition either by pharmacologic inhibitors or RNAi-mediated gene silencing
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G651939-10mgGDC-0425 (RG-7602) is an orally available, highly selective small molecule ChK1 inhibitor. GDC-0425 can be used for the research of various malignanciesIn VitroMEK inhibition either by pharmacologic inhibitors or RNAi-mediated gene silencing
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G651939-25mgGDC-0425 (RG-7602) is an orally available, highly selective small molecule ChK1 inhibitor. GDC-0425 can be used for the research of various malignanciesIn VitroMEK inhibition either by pharmacologic inhibitors or RNAi-mediated gene silencing