Protease Inhibitors and Phosphatase Inhibitors
Abcam MG-132, proteasome inhibitor, 5MG
MW 475.6 Da, Purity >98%. MG-132, proteasome inhibitor. Achieve your results faster with highly validated, pure and trusted compounds.
The product is subject to the following: Abcam Restricted Use Statement
CPC Scientific MCA-Pro-Cha-Gly-Nva-His-Ala-Dap(DNP)-NH2 (trifluoroacetate salt) 0.5MG
Specific fluorogenic substrate for collagenase-3 (MMP) with a kcat/Km value of 1.09 x 106 M-1s-1 (pH = 7.5, T = 25 °C, substrate concentrations: 0.7 and 1.4 µM (S<
Cayman Chemical Cdk2 InhIbItr II 500ug
A 3-(benzylidne)indolin-2-one analog that selectively and potently inhibits Cdk2 (IC50 = 60 nM)
AURORA BIOLABS LLC PD-1/PD-L1 Inhibitor Binding Asssay Kit, 384 rxn
PD-1/PD-L1 Inhibitor Binding Asssay Kit, 384 rxn
Supply Solutions PhosSTOP™ 10 tablets
PhosSTOP tablets are a proprietary blend of phosphatase inhibitors, formulated as a ready-to-use tablet which dissolves quickly in aqueous solutions (buffers), including buffers containing formalin (for formalin fixation).
Vector Biolabs Protein phosphatase 1 catalytic subunit alpha isoform Adenovirus (Ad-PP-1A)
Ready to use in vivo grade AAV and Adenovirus Ready to use in vivo grade AAV and Adenovirus pre synthesized DNA vector High titer viral vectors 1/EA
Vector Biolabs Protein phosphatase 3 (formerly 2B) catalytic subunit gamma isoform (calcineurin A gamma) Adenovirus (Ad-PP2B/CALNA3)
Ready to use in vivo grade AAV and Adenovirus Ready to use in vivo grade AAV and Adenovirus pre synthesized DNA vector High titer viral vectors 1/EA
Abcam RKRARKE, PKG Inhibitor, 1MG
MW 943.12 g/mol, Purity >99%. Competitive protein kinase G (PKG) inhibitor. Ki = 86 µM for PKG; Ki = 550 µM for PKA. Potential inhibitory activity in neuronal systems.
The product is subject to the following: Abcam Restricted Use Statement
Abcam p-Nitropifithrin-alpha, p53 inhibitor, 5MG
MW 398.3 Da, Purity >98%. Cell-permeable p53 inhibitor. Pifithrin-α (ab120478) analog and prodrug. Shows more potent antiapoptotic effects than pifithrin-α. Shows antiobesogenic and hepatoprotective effects in vivo. .
The product is subject to the following: Abcam Restricted Use Statement
Cayman Chemical IL-4 InhIbItr 5mg
An IL-4 inhibitor; binds to IL-4 (Kd = 1.8 μM); inhibits IL-4 activity in a cell-based reporter assay (EC50 = 1.81 μM); selective for IL-4 over IL-13 (EC50 = 18.2 μM); inhibits IL-4-induced STAT6 phosphorylation in THP-1 monocytes (EC50 = 3.1 μM)
Vector Biolabs mouse FOS shRNA Adenovirus (Ad-m-FOS-shRNA)
Ready to use in vivo grade AAV and Adenovirus Ready to use in vivo grade AAV and Adenovirus pre synthesized DNA vector High titer viral vectors 1/EA
Cayman Chemical nDD8 InhIbItr M22 1mg
An inhibitor of NEDD8-activating enzyme; inhibits NEDDylation of UBC12 in a cell-free assay using recombinant human NAE; selectively inhibits NEDDylation over SUMOylation and ubiquitination in A549 cells; inhibits the growth of A549 cells (GI50 = 5.5 µM); inhibits tumor growth in an AGS gastric adenocarcinoma mouse xenograft model at 60 mg/kg
Medchemexpress LLC RBPJ Inhibitor-1 (RIN1) | 2682114-39-0 | 99.9% | 311.31 | 50 MG
RBPJ Inhibitor-1 (RIN1) is the first RBPJ inhibitor, which blocks the functional interaction of RBPJ with SHARP. It inhibits NOTCH-dependent tumor cell proliferation and is intended for research use only.
- Blocks the functional interaction of RBPJ with SHARP
- Inhibits NOTCH-dependent tumor cell proliferation
- Inhibits the proliferation of hematologic cancer cell lines
- Promotes skeletal muscle differentiation from C2C12 myoblasts
Apexbio Technology LLC Cell-permeable, and irreversible caspase-3 inhibitor 210344-95-9. MFCD23380217
Cell-permeable, and irreversible caspase-3 inhibitor 210344-95-9. MFCD23380217