Biochemical Compounds

Ideal for mycotoxin analyses in cannabis and food testing labs.

Cell Line Origin Rat Y3Ag1.2.

Cell Line Origin Rat Y3Ag1.2.

Cell Line Origin Rat Y3Ag1.2.

Cell Line Origin Rat Y3Ag1.2.

Cell Line Origin Rat YB2/3.0 Ag20 x Rat F344 spleen Cell Line Description The antibody is directed against NADH nitrate reductase of spinach and marrow.

Cell Line Origin Rat YB2/3.0 Ag20 x Rat F344 spleen Cell Line Description The antibody is specific for NADH-nitrate reductase of spinach and marrow.

A cell-permeable pyrazolo-amide compound that potently blocks the binding of TCDD (2,3,7,8-tetrachlorodibenzo- p -dioxin) to AhR (aryl hydrocarbon receptor) in a dose-dependent manner. Shown to Inhibit TCDD-induced AhR transcription activity in

A cell-permeable purine compound that acts as a high affinity (IC 50 = 40 nM against [125I]-N3Br2DD binding to human AhR) AhR antagonist (IC 50 = 127 nM against 3 nM TCDD-induced luciferase reporter activity in HepG2 cultures), while exhibiting

A cell-permeable purine compound that acts as a high-affinity aryl hydrocarbon receptor (AhR) antagonist (IC 50 = 62 nM in mouse liver cytosol expressing humanized AhR) and lacks any agonist activity even at higher doses. Reportedly binds with high

A cell permeable, reversible, and substrate competitive phosphatidylinositol analog that inhibits the activation of Akt and select downstream substrates without decreasing phosphorylation of PDK-1 or other kinases downstream of Ras, such as MAPK.

A cell-permeable and reversible quinoxaline compound that potently and selectively inhibits Akt1/Akt2 activity (IC 50 = 58 nM, 210 nM, and 2.12 &#181M for Akt1, Akt2, and Akt3, respectively, in in vitro kinase assays).