Bleomycin

Tenascin is known to play an active role in development of central nervous system and mesenchymal-derived organs, exist in the vasculature of tumors in adults, and function in cell adhesion. Specificity Reactivity with other species has not been

Actinomycin D: Classical anti-neoplastic drug. Cytotoxic inducer of apoptosis against tumor cells.

Atuveciclib (BAY-1143572) is a potent and highly selective, oral PTEFb / CDK9 inhibitor. Atuveciclib (BAY-1143572) inhibits CDK9 / CycT1 with an IC 50 of 13 nM.Appearance:SolidIC50&amp: Target:CDK9/CycT1 13 nM (IC 50 ) CDK9/CycT1(h) 6 nM (IC 50 )

Atuveciclib (BAY-1143572) is a potent and highly selective, oral PTEFb / CDK9 inhibitor. Atuveciclib (BAY-1143572) inhibits CDK9 / CycT1 with an IC 50 of 13 nM.Appearance:SolidIC50&amp: Target:CDK9/CycT1 13 nM (IC 50 ) CDK9/CycT1(h) 6 nM (IC 50 )

Atuveciclib (BAY-1143572) is a potent and highly selective, oral PTEFb / CDK9 inhibitor. Atuveciclib (BAY-1143572) inhibits CDK9 / CycT1 with an IC 50 of 13 nM.Appearance:SolidIC50&amp: Target:CDK9/CycT1 13 nM (IC 50 ) CDK9/CycT1(h) 6 nM (IC 50 )

Onguard Vial Adaptor, 20mm, ES, 50/bx, 4 bx/cs (Rx) (Continental US+HI Only)

Bafilomycin A1 is a potent and selective inhibitor of V-ATPase (vacuolar-type (v-type) H+ ATPase) and belongs to a class of membrane ATPase inhibitors. The compound can inhibit E1E2 ATPases from sarcoplasmic reticulum, Escherichia coli, and ox brain

Bafilomycin A1 is a potent and selective inhibitor of V-ATPase (vacuolar-type (v-type) H+ ATPase) and belongs to a class of membrane ATPase inhibitors. The compound can inhibit E1E2 ATPases from sarcoplasmic reticulum, Escherichia coli, and ox brain

Bafilomycin A1

Bafilomycin A1

Sensi-Disc Erythromycin E-15 (Perishable Product: Must be Refrigerated: Non-Returnable) (Continental US Only) (Drop Ship Requires Pre-Approval)

Biochem/physiol Actions BH3I-1is a synthetic cell permeable Bcl-x L antagonist apoptosis inducer.