纯度规格：The PKG Inhibitor controls the biological activity of PKG. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
纯度规格：PP1 Analog II, CAS 221244-14-0, is a cell-permeable PP1 analog that acts as a potent, reversible, selective, ATP-competitive inhibitor of mutant over wild-type kinases.
纯度规格：The Proteasome Inhibitor Set I controls the biological activity of Proteasome. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.
纯度规格：The Proteasome Inhibitor Set II controls the biological activity of Proteasome. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.
纯度规格：The Raf1 Kinase Inhibitor I, also referenced under CAS 220904-83-6, controls the biological activity of Raf1 Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
纯度规格：A potent, selective, and competitive antagonist of the G-protein coupled receptor CXCR2 (IL-8RB; IC
50= 22 nM for the inhibition of
125I-IL-8 binding to CXCR2).
纯度规格：The Serine/Threonine Kinase Inhibitor Set controls the biological activity of Serine/Threonine Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
纯度规格：Cell permeable. Blocks glibenclamide-sensitive K
+channels. Inhibits neuronal nitric oxide synthase. Also inhibits hepatic drug metabolism by inhibiting the cytochrome P450 system.
纯度规格：The Smac-
N7 peptide is modified to be cell permeant by linking the lysine carboxyl terminal to the arginine of Antennapedia homeodomain 16-mer peptide via a proline linker.
纯度规格：A pentavalent antimony compound that irreversibly inhibits protein tyrosine phosphatase (PTPase) activity, including Src homology PTPase-1 (SHP-1) (99% inhibition at ~11 μM) by forming a stable complex.
纯度规格：The sPLA
2-IIA Inhibitor I controls the biological activity of sPLA
2-IIA. This small molecule/inhibitor is primarily used for Cell Signaling applications.
纯度规格：TAPI-1, CAS 171235-71-5, is a structural analog of TAPI-0 with similar
in vitroefficacy for the inhibition of MMPs and TACE. Blocks the shedding of several cell surface proteins.
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