Tubocurarine chloride

CD31 Rat mAb (FITC)

InformationChlormezanone，a non-benzodiazepine that is used in the management of anxiety. It has been suggested for use in the treatment of muscle spasm.In vitroIn vivoCell Datacell lines：K562, BaF3/wt, BaF3/E255K, and BaF3/T315I

Antigen: fusion protein amino acids 761-863 (cytoplasmic C-terminus) of rat HCN2 Host: mouse, clone S71-37 Isotype: IgG1 Cross Reactivity: (+) human and rat HCN2 Application(s): ICC, IHC, IP, and WB Hyperpolarization-activated cation channels of the

Iptacopan (LNP023) is a first-in-class, orally bioavailable, highly potent and highly selective factor B inhibitor with an IC 50 value of 10 nM. Iptacopan shows direct, reversible, and high-affinity binding to human factor B with a K D of 7.9 nM.

An inactive stereoisomer (IC₅₀ &ge 1 mM) of the Cdk5 inhibitor olomoucine may have utility as a control compound for determining Cdk5 specificity rapidly inhibits dopamine transporter activity in rat dorsal striatal synaptosomes with

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A potent, selective inhibitor of HDAC6 (IC₅₀ = 5.02 nM) dose-dependently induces hyperacetylation of &alpha-tubulin in B16 murine melanoma cells without elevating histone H3 acetylation.

PF-8380 is a potent and specific autotaxin inhibitor with an IC50 value of 2.8 nM.A substrate competitive and tight-binding inhibitor of autotaxin.

PF-8380 is a potent and specific autotaxin inhibitor with an IC50 value of 2.8 nM.A substrate competitive and tight-binding inhibitor of autotaxin.

Application Suitable for thermocouple use Quantity 180 mg = 1 m 900 mg = 5 m

Application Suitable for thermocouple use Quantity 180 mg = 1 m 900 mg = 5 m

Pranidipine is a is a long-acting dihydropyridine calcium channel blocker antagonist for use as an antihypertensive agent. Pranidipine has a high affinity for Ca channels or for T-tubule membranes, and strongly supports the membrane-bilayer pathway"