Assay Testing Coq10 As Ubiquinone

Lab Reagents

Coq10 Assay Laboratories manufactures the assay testing coq10 as ubiquinone reagents distributed by Genprice. The Assay Testing Coq10 As Ubiquinone reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact coq10 assay. Other Assay products are available in stock. Specificity: Assay Category: Testing Group: Coq10 As

Coq10 As information

AS-252424

B2180-5 5 mg
EUR 131
Description: AS-252424 is a potent, selective and novel small-molecule PI3K? inhibitor (IC50= 30 nM) PI3K (phosphatidylinositol-4,5-bisphosphate 3-kinase) is a family of enzymes involved in cellular functions such as cell growth, proliferation, differentiation, motility, survival and intracellular trafficking.

AS-252424

B2180-S Evaluation Sample
EUR 81
Description: AS-252424 is a potent, selective and novel small-molecule PI3K? inhibitor (IC50= 30 nM) PI3K (phosphatidylinositol-4,5-bisphosphate 3-kinase) is a family of enzymes involved in cellular functions such as cell growth, proliferation, differentiation, motility, survival and intracellular trafficking.

AS-604850

B2181-10 10 mg
EUR 273
Description: AS-604850 is a selective and ATP-competitive PI3K? inhibitor (IC50= 2.5 ?M), with over 30-fold selectivity for PI3K? and PI3K?, and 18-fold selectivity over PI3K?.

AS-604850

B2181-25 25 mg
EUR 537
Description: AS-604850 is a selective and ATP-competitive PI3K? inhibitor (IC50= 2.5 ?M), with over 30-fold selectivity for PI3K? and PI3K?, and 18-fold selectivity over PI3K?.

AS-604850

B2181-5 5 mg
EUR 174
Description: AS-604850 is a selective and ATP-competitive PI3K? inhibitor (IC50= 2.5 ?M), with over 30-fold selectivity for PI3K? and PI3K?, and 18-fold selectivity over PI3K?.

AS 1892802

B5773-10 10 mg
EUR 373
Description: AS 1892802 is a potent and selective inhibitor of ROCK with IC50 values of 52, 57 and 122 nM for human ROCK2, rat ROCK2 and human ROCK1, respectively [1]. Rho kinase (ROCK) is a serine-threonine kinase and is a downstream effector of Rho, a small GTP-bound protein.

AS 1892802

B5773-25 25 mg
EUR 757
Description: AS 1892802 is a potent and selective inhibitor of ROCK with IC50 values of 52, 57 and 122 nM for human ROCK2, rat ROCK2 and human ROCK1, respectively [1]. Rho kinase (ROCK) is a serine-threonine kinase and is a downstream effector of Rho, a small GTP-bound protein.

AS 1892802

B5773-5 5 mg
EUR 232
Description: AS 1892802 is a potent and selective inhibitor of ROCK with IC50 values of 52, 57 and 122 nM for human ROCK2, rat ROCK2 and human ROCK1, respectively [1]. Rho kinase (ROCK) is a serine-threonine kinase and is a downstream effector of Rho, a small GTP-bound protein.

AS 19

B6902-10 10 mg
EUR 373
Description: AS 19 is a potential 5-HT7 receptor agonist with an IC50 value of 0.83 nM [1].5-HT7 receptor plays a role in the control of both sleep and circadian rhythms.

AS 19

B6902-50 50 mg
EUR 1363
Description: AS 19 is a potential 5-HT7 receptor agonist with an IC50 value of 0.83 nM [1].5-HT7 receptor plays a role in the control of both sleep and circadian rhythms.

AS-252424

B1611-25
EUR 1436

AS-252424

B1611-5
EUR 457

AS 1949490

B7483-10 10 mg
EUR 231
Description: AS 1949490 is a selective inhibitor of Src homology 2 domain-containing inositol-5-phosphatase 2 (SHIP2), [1] with IC50 values of 0.34 µM and 0.62 µM to mouse and human SHIP2s, respectively [2].

AS 1949490

B7483-5 5 mg
EUR 154
Description: AS 1949490 is a selective inhibitor of Src homology 2 domain-containing inositol-5-phosphatase 2 (SHIP2), [1] with IC50 values of 0.34 µM and 0.62 µM to mouse and human SHIP2s, respectively [2].

AS 1949490

B7483-50 50 mg
EUR 833
Description: AS 1949490 is a selective inhibitor of Src homology 2 domain-containing inositol-5-phosphatase 2 (SHIP2), [1] with IC50 values of 0.34 µM and 0.62 µM to mouse and human SHIP2s, respectively [2].

AS 1269574

B7606-10 10 mg
EUR 181
Description: AS 1269574,(2-[2-(4-bromophenyl)-6-methylpyrimidin-4-yl] amino ethanol), was capable of inducing glucose-stimulated insulin secretion (GSIS) and improved glucose tolerance in normal mice. AS 1269574 is an agonist of GPR119 with EC50 value of 2.5 µM [1] [2].

AS 1269574

B7606-25 25 mg
EUR 342
Description: AS 1269574,(2-[2-(4-bromophenyl)-6-methylpyrimidin-4-yl] amino ethanol), was capable of inducing glucose-stimulated insulin secretion (GSIS) and improved glucose tolerance in normal mice. AS 1269574 is an agonist of GPR119 with EC50 value of 2.5 µM [1] [2].