Apexbio Manufacturer Part Number A8192

Staurosporine

A8192-1 1 mg
EUR 129.6
Description: Staurosporine, an alkaloid produced in Streptomyces staurospores originally as an antifungal agent, is an inhibitor of a broad spectrum of protein kinases, including protein kinase C (PKC), Camp-dependent protein kinase (PKA), phosphorylase kinase, ribosomal protein S6 kinase and (Ca/CaM PKII).

Apexbio Reagents Laboratories manufactures the apexbio manufacturer part number a8192 reagents distributed by Genprice. The Apexbio Manufacturer Part Number A8192 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: Manufacturer Group: Part Number

Part Number information

DNAzymeMB (Part of Lysozyme Aptasensor), DNA Aptamer, Biotinylated

AD-128-B Custom Ask for price

DNAzymeMB (Part of Lysozyme Aptasensor), DNA Aptamer, unlabeled

AD-128-U Custom Ask for price

Alveolar Soft Part Sarcoma Chromosome Region, Candidate 1

PR27224 2 ug
EUR 229.2

DNAzymeMB (Part of Lysozyme Aptasensor), DNA Aptamer, FITC labeled

AD-128-F Custom Ask for price

Alveolar Soft Part Sarcoma Chromosome Region, Candidate 1 Protein

20-abx263361
  • EUR 1930.80
  • EUR 393.60
  • EUR 276.00
  • 100 ug
  • 10 ug
  • 2 µg

ASPSCR1 Alveolar Soft Part Sarcoma Chromosome Region, Candidate 1 Human Recombinant Protein

PROTQ9BZE9 Regular: 10ug
EUR 380.4
Description: ASPSCR1 Human Recombinant produced in E. coli is a single polypeptide chain containing 576 amino acids (1-553) and having a molecular mass of 62.6kDa. ASPSCR1 is fused to a 23 amino acid His-tag at N-terminus & purified by proprietary chromatographic techniques.

Exosomal Protein Lysis Buffer

P200P,-part-of-P200 - Ask for price

Exosomal RNA Extraction Kit

P200R,-part-of-P200 - Ask for price

CX-5461

A8337-50 50 mg
EUR 811.2
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.

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.