Agrisera As 09602

Lab Reagents

Agrisera Plant Antibodies Laboratories manufactures the agrisera as 09602 reagents distributed by Genprice. The Agrisera As 09602 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 Agrisera Plant Antibodies. Other Agrisera products are available in stock. Specificity: Agrisera Category: As Group: 9602

9602 information

AS-605240

A5176-100 100 mg
EUR 374
Description: AS-605240 is a selective PI3K ? inhibitor with an IC50 of 8 nM. [1]PI3Ks are a family of enzymes, which phosphorylate the 3?- OH position of the inositol ring of phosphoinositides.

AS-605240

A5176-5.1 10 mM (in 1mL DMSO)
EUR 113
Description: AS-605240 is a selective PI3K ? inhibitor with an IC50 of 8 nM. [1]PI3Ks are a family of enzymes, which phosphorylate the 3?- OH position of the inositol ring of phosphoinositides.

AS-605240

A5176-50 50 mg
EUR 276
Description: AS-605240 is a selective PI3K ? inhibitor with an IC50 of 8 nM. [1]PI3Ks are a family of enzymes, which phosphorylate the 3?- OH position of the inositol ring of phosphoinositides.

AS 602801

A3189-10 10 mg
EUR 347
Description: Kinases represent one of the most popular and promising target class in drug discovery. Success in finding new therapeutics will depend on the validation of the kinase chosen with respect to the disease of interest, and on the ability of chemists to design and synthesize inhibitors.

AS 602801

A3189-200 200 mg
EUR 1362
Description: Kinases represent one of the most popular and promising target class in drug discovery. Success in finding new therapeutics will depend on the validation of the kinase chosen with respect to the disease of interest, and on the ability of chemists to design and synthesize inhibitors.

AS 602801

A3189-5.1 10 mM (in 1mL DMSO)
EUR 334
Description: Kinases represent one of the most popular and promising target class in drug discovery. Success in finding new therapeutics will depend on the validation of the kinase chosen with respect to the disease of interest, and on the ability of chemists to design and synthesize inhibitors.

AS 602801

A3189-50 50 mg
EUR 527
Description: Kinases represent one of the most popular and promising target class in drug discovery. Success in finding new therapeutics will depend on the validation of the kinase chosen with respect to the disease of interest, and on the ability of chemists to design and synthesize inhibitors.

AS 602801

A3189-500 500 mg
EUR 2436
Description: Kinases represent one of the most popular and promising target class in drug discovery. Success in finding new therapeutics will depend on the validation of the kinase chosen with respect to the disease of interest, and on the ability of chemists to design and synthesize inhibitors.

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].

AS 1269574

B7606-5 5 mg
EUR 154
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 2034178

B7735-10 10 mg
EUR 373
Description: AS2034178 is a GPR40 agonist [1] with an hEC50 value of 380 nM [2].GPR40 is a receptor of free fatty acid. It regulates glucose-dependent insulin secretion [1].AS2034178 can improve glucose homeostasis and maintain or enhance islet beta cell functions [3].

AS 2034178

B7735-50 50 mg
EUR 1363
Description: AS2034178 is a GPR40 agonist [1] with an hEC50 value of 380 nM [2].GPR40 is a receptor of free fatty acid. It regulates glucose-dependent insulin secretion [1].AS2034178 can improve glucose homeostasis and maintain or enhance islet beta cell functions [3].

AS 101

B7830-5 5 mg
EUR 171
Description: Ammonium tri-chloro(dioxoethylene-O,O?-)tellurate (AS-101), an anti?IL-10 compound, is a nontoxic immunomodulator.AS101 (0.43222.5 ?g/ml) decreased IL-10 production in a dose-dependent manner.