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C153267-250mgCalcium Dobesilate Hydrate.
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C153267-25gCalcium Dobesilate Hydrate.
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C153267-5gCalcium Dobesilate Hydrate.
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C658909-10mgCaloxin 2A1 TFA is an extracellular plasma membrane Ca 2+ -ATPase (PMCA) peptide inhibitor. Caloxin 2A1 TFA does not affect basal Mg 2+ -ATPase or Na + -K + -ATPase.Appearance:SolidIn Vitro:Caloxin 2A1 TFA inhibits Ca 2+ -Mg 2+ -ATPase in human
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C658909-1mgCaloxin 2A1 TFA is an extracellular plasma membrane Ca 2+ -ATPase (PMCA) peptide inhibitor. Caloxin 2A1 TFA does not affect basal Mg 2+ -ATPase or Na + -K + -ATPase.Appearance:SolidIn Vitro:Caloxin 2A1 TFA inhibits Ca 2+ -Mg 2+ -ATPase in human
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C658909-25mgCaloxin 2A1 TFA is an extracellular plasma membrane Ca 2+ -ATPase (PMCA) peptide inhibitor. Caloxin 2A1 TFA does not affect basal Mg 2+ -ATPase or Na + -K + -ATPase.Appearance:SolidIn Vitro:Caloxin 2A1 TFA inhibits Ca 2+ -Mg 2+ -ATPase in human
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C658909-50mgCaloxin 2A1 TFA is an extracellular plasma membrane Ca 2+ -ATPase (PMCA) peptide inhibitor. Caloxin 2A1 TFA does not affect basal Mg 2+ -ATPase or Na + -K + -ATPase.Appearance:SolidIn Vitro:Caloxin 2A1 TFA inhibits Ca 2+ -Mg 2+ -ATPase in human
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C658909-5mgCaloxin 2A1 TFA is an extracellular plasma membrane Ca 2+ -ATPase (PMCA) peptide inhibitor. Caloxin 2A1 TFA does not affect basal Mg 2+ -ATPase or Na + -K + -ATPase.Appearance:SolidIn Vitro:Caloxin 2A1 TFA inhibits Ca 2+ -Mg 2+ -ATPase in human
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C649440-10mgCalpain-2-IN-1 (Formula 1A) is a isoform-specific calpain-2 inhibitor with K i s of 181 nM and 7.8 nM for calpain-1, and calpain-2, respectively. Calpain-2-IN-1 can be used for the research of neurodegenerative diseases and other diseases of
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C649440-5mgCalpain-2-IN-1 (Formula 1A) is a isoform-specific calpain-2 inhibitor with K i s of 181 nM and 7.8 nM for calpain-1, and calpain-2, respectively. Calpain-2-IN-1 can be used for the research of neurodegenerative diseases and other diseases of
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C650141-10mgCAM833 is a potent orthosteric inhibitor of the interaction between BRCA2 and RAD51 with a K d of 366 nM against the ChimRAD51 protein. CAM833 also inhibits RAD51 oligomerization. CAM833 increases the progression of G2/M-arrested cells into
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C650141-25mgCAM833 is a potent orthosteric inhibitor of the interaction between BRCA2 and RAD51 with a K d of 366 nM against the ChimRAD51 protein. CAM833 also inhibits RAD51 oligomerization. CAM833 increases the progression of G2/M-arrested cells into