Apexbio Paclitaxel

Paclitaxel (Taxol)
A4393-100 100 mg
EUR 170.4
Description: Paclitaxel is a novel antineoplastic agent, which was discovered in a screen of extracts of thousands of plants and natural products for antineoplastic activity by a National Cancer Institute program

Apexbio Reagents Laboratories manufactures the apexbio paclitaxel reagents distributed by Genprice. The Apexbio Paclitaxel 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 Apexbio Reagents. Other Apexbio products are available in stock. Specificity: Apexbio Category: Paclitaxel

Human Samples information

CX-5461
A8337-S Evaluation Sample
EUR 97.2
Description: CX-5461 is a potent and orally bioavailable small-molecule inhibitor of rRNA synthesis that specifically inhibits RNA polymerase (Pol) I-driven transcription with IC50 value of 142 nM.

NSC 74859
A8338-10 10 mg
EUR 157.2
Description: S3I-201 is a selective inhibitor of Stat3 with IC50 value of 86 ?M [1].In the in vitro Stat3 DNA-binding assay, S3I-201 showed potent inhibition of the Stat3 DNA-binding activity with an average IC50 of 86 ?M.

NSC 74859
A8338-200 200 mg
EUR 793.2
Description: S3I-201 is a selective inhibitor of Stat3 with IC50 value of 86 ?M [1].In the in vitro Stat3 DNA-binding assay, S3I-201 showed potent inhibition of the Stat3 DNA-binding activity with an average IC50 of 86 ?M.

NSC 74859
A8338-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: S3I-201 is a selective inhibitor of Stat3 with IC50 value of 86 ?M [1].In the in vitro Stat3 DNA-binding assay, S3I-201 showed potent inhibition of the Stat3 DNA-binding activity with an average IC50 of 86 ?M.

NSC 74859
A8338-50 50 mg
EUR 304.8
Description: S3I-201 is a selective inhibitor of Stat3 with IC50 value of 86 ?M [1].In the in vitro Stat3 DNA-binding assay, S3I-201 showed potent inhibition of the Stat3 DNA-binding activity with an average IC50 of 86 ?M.

NSC 74859
A8338-S Evaluation Sample
EUR 97.2
Description: S3I-201 is a selective inhibitor of Stat3 with IC50 value of 86 ?M [1].In the in vitro Stat3 DNA-binding assay, S3I-201 showed potent inhibition of the Stat3 DNA-binding activity with an average IC50 of 86 ?M.

TAK-875
A8339-10 10 mg
EUR 366
Description: TAK-875 is a potent, selective, and oral GPR40 agonist. GPR40 is one of the G protein-coupled receptors predominantly expressed in pancreatic ?-cells, mediating enhancement of glucose-stimulated insulin secretion by free fatty acids.

TAK-875
A8339-5 5 mg
EUR 226.8
Description: TAK-875 is a potent, selective, and oral GPR40 agonist. GPR40 is one of the G protein-coupled receptors predominantly expressed in pancreatic ?-cells, mediating enhancement of glucose-stimulated insulin secretion by free fatty acids.

TAK-875
A8339-5.1 10 mM (in 1mL DMSO)
EUR 268.8
Description: TAK-875 is a potent, selective, and oral GPR40 agonist. GPR40 is one of the G protein-coupled receptors predominantly expressed in pancreatic ?-cells, mediating enhancement of glucose-stimulated insulin secretion by free fatty acids.

TAK-875
A8339-50 50 mg
EUR 714
Description: TAK-875 is a potent, selective, and oral GPR40 agonist. GPR40 is one of the G protein-coupled receptors predominantly expressed in pancreatic ?-cells, mediating enhancement of glucose-stimulated insulin secretion by free fatty acids.

TAK-875
A8339-S Evaluation Sample
EUR 97.2
Description: TAK-875 is a potent, selective, and oral GPR40 agonist. GPR40 is one of the G protein-coupled receptors predominantly expressed in pancreatic ?-cells, mediating enhancement of glucose-stimulated insulin secretion by free fatty acids.

Cyclopamine
A8340-10 10 mg
EUR 150
Description: Cyclopamine is a naturally occurring Hedgehog (Hh)?specific small?molecule signaling steroidal alkaloid inhibitor, causes a profound inhibition of tumor growth, has significant anti?invasive, anti?proliferative and anti?estrogenic potency in human breast cancer cells [2] [1].

Cyclopamine
A8340-25 25 mg
EUR 199.2
Description: Cyclopamine is a naturally occurring Hedgehog (Hh)?specific small?molecule signaling steroidal alkaloid inhibitor, causes a profound inhibition of tumor growth, has significant anti?invasive, anti?proliferative and anti?estrogenic potency in human breast cancer cells [2] [1].

Cyclopamine
A8340-5 5 mg
EUR 129.6
Description: Cyclopamine is a naturally occurring Hedgehog (Hh)?specific small?molecule signaling steroidal alkaloid inhibitor, causes a profound inhibition of tumor growth, has significant anti?invasive, anti?proliferative and anti?estrogenic potency in human breast cancer cells [2] [1].

Cyclopamine
A8340-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: Cyclopamine is a naturally occurring Hedgehog (Hh)?specific small?molecule signaling steroidal alkaloid inhibitor, causes a profound inhibition of tumor growth, has significant anti?invasive, anti?proliferative and anti?estrogenic potency in human breast cancer cells [2] [1].

Cyclopamine
A8340-S Evaluation Sample
EUR 97.2
Description: Cyclopamine is a naturally occurring Hedgehog (Hh)?specific small?molecule signaling steroidal alkaloid inhibitor, causes a profound inhibition of tumor growth, has significant anti?invasive, anti?proliferative and anti?estrogenic potency in human breast cancer cells [2] [1].

Go 6976
A8341-1 1 mg
EUR 172.8
Description: Go 6976 is a selective inhibitor of PKC with IC50 value of 20 nM [1] [2].