Microarray Kits
AMERICAN RESEARCH PRODUCTS INC THUNDERCELL SIGNALING ASSAYKIT
NC2374162 THUNDERCELL SIGNALING ASSAYKIT
Biotium Catenin gamma Cardiomyocyte Marker 11 E4 CF568 conjugate 0.1mgmL
Catenin gamma Cardiomyocyte Marker 11 E4 CF568 conjugate 0.1mgmL
Abcam SMER3, SCFMet30 ubiquitin E3 ligase inhibitor, 10MG
MW 224.17 Da, Purity >98%. Cell permeable, selective SCFMet30 ubiquitin E3 ligase inhibitor. Enhances the action of rapamycin. Induces cell cycles arrest (IC50 = 10-30 μM). Active *in vivo.*.
The product is subject to the following: Abcam Restricted Use Statement
Cayman Chemical UbIquItIn Iso PEP InHBI 25mg
A selective inhibitor of SHP-2 (IC50 2 1 UM Ki 0 73 UM) inhibits SHP-2-dependent cellular signaling and tumor cell colony formation
Cayman Chemical JWH 081 7methoxynaphthyl5mg
An antagonist of NR1A/2B subunit-containing NMDA receptors (IC50 0.0053 UM) selective for NMDA receptors containing NR1A/2B subunits over NMDA receptors containing NR1A/2A and NR1A/2C subunits (IC50s 35 and >100 UM respectively) inhibits L-DOPA-induced contralateral rotations in a rat model of 6-OHDA-induced Parkinson's disease at 10 mg/kg has been radiolabeled and used as an NR1A/2B-selective PET radiotracer
Cayman Chemical JWH 081 2methoxynaphthyl10mg
A fluorogenic substrate for prolyl endopeptidase AMC is released upon enzymatic cleavage by prolyl endopeptidase and its fluorescence can be used to quantify prolyl endopeptidase activity ex/em 340-360/440-460 nm respectively
Cayman Chemical JWH 081 6methoxynaphthyl10mg
A urotensin II receptor antagonist (Kis 61 17 30 65 and 56 nM for the human monkey cat rat and mouse receptors respectively) reduces urotensin II-induced increases in the expression of IL1B IL6 and VCAM1 in EA.hy926 cells at 1 UM reduces urotensin II-induced adhesion of U937 monocytes to EA.hy926 cells at 1 UM
Cayman Chemical JWH 081 3methoxynaphthyl10mg
A fluorogenic substrate for prolyl endopeptidase AMC is released upon enzymatic cleavage by prolyl endopeptidase and its fluorescence can be used to quantify prolyl endopeptidase activity ex/em 340-360/440-460 nm respectively
Cayman Chemical JWH 081 8methoxynaphthyl10mg
A urotensin II receptor antagonist (Kis 61 17 30 65 and 56 nM for the human monkey cat rat and mouse receptors respectively) reduces urotensin II-induced increases in the expression of IL1B IL6 and VCAM1 in EA.hy926 cells at 1 UM reduces urotensin II-induced adhesion of U937 monocytes to EA.hy926 cells at 1 UM
Cayman Chemical JWH 081 NpentnoIc ACD meta 5mg
A potent synthetic CB activating the CB1 receptor with a Ki value of 4 5 nM and the CB2 receptor with a Ki value of 1 88 nM effects in cells and animals are unknown intended for research and forensic applications
Cayman Chemical JWH 081 N 5hydroxypentyl m
An inhibitor of RGS4 (IC50 30 nM) blocks GTPase activity and Ga0-dependent translocation of RGS4 to the membrane