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Tissue membrane protein is prepared from whole tissue homogenates and presents a consistent pattern on SDS-PAGE analysis. The protein is stored in a buffer with protease inhibitor cocktail.
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Wortmannin (KY 12420) is the first described PI3K inhibitor with IC50 of 3 nM in a cell-free assay, with little selectivity within the PI3K family. Wortmannin blocks autophagosome formation and potently inhibits DNA-PK/ATM with IC50 of 16 nM and 150 nM in cell-free assays. Wortmannin also inhibits PLK1 activity. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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NSC668394 is a small-molecule ezrin phosphorylation inhibitor used in preclinical research to study ezrin-dependent signaling and metastatic processes. It binds ezrin and reduces Thr567 phosphorylation, affecting cytoskeleton-associated signaling pathways.
Inhibits ezrin Thr567 phosphorylation and ezrin-mediated signaling.
Suitable for in vitro, cell-based studies due to cell permeability.
High reported purity (99.31%) for reliable experimental results.
Available as a solid and as a 10 mM solution in DMSO for convenience.
Molecular weight 452.10 g·mol⁻¹; formula C17H12Br2N2O3.
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Medchemexpress, HY-K0206 1 mL Anti-c-Myc Magnetic Beads CAS: Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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An NNMT inhibitor (IC50 = 1.41 µM); binds the NNMT active site in the binding pockets for SAM and nicotinamide; selective for NNMT over NSD2 and PRMT1 (IC50s = >50 µM for both); reduces MNA levels in, and inhibits proliferation of, HSC-2 oral cancer cells at 100 µM
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ExoBrite CD9/CD63/CD81 3-Color Antibody Cocktail (Blue/Green/Far-Red) consists of three tetraspanin antibody dye conjugates in a single tube Designed for EV phenotyping by flow cytometry
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PKC-theta inhibitor 2 is a potent and selective PKC-θ inhibitor with an IC50 value of 18 nM. It is a 2,4-diamino-5-nitropyrimidine compound with the 2-position substituted by o-trifluoromethoxy.
Potent and selective PKC-θ inhibitor.
For research use only.
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