American Journal of Engineering & Natural Sciences (AJENS) ISSN 2074-112X

Original Research Contributions in Genetic Biongineering And Natural Genome Editing

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Eatpase Inhibitor

Lab Reagents

Activation Assay Laboratories manufactures the eatpase inhibitor reagents distributed by Genprice. The Eatpase Inhibitor 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 activation assay. Other Eatpase products are available in stock. Specificity: Eatpase Category: Inhibitor

Serum / Plasma information

STAT5 Inhibitor

C4105-10 10 mg
EUR 196
Description: STAT5 Inhibitor is a cell-permeable inhibitor of STAT5 with IC50 value of 47 ?M against STAT5? SH2 domain EPO peptide binding activity [1].

STAT5 Inhibitor

C4105-25 25 mg
EUR 376
Description: STAT5 Inhibitor is a cell-permeable inhibitor of STAT5 with IC50 value of 47 ?M against STAT5? SH2 domain EPO peptide binding activity [1].

STAT5 Inhibitor

C4105-5 5 mg
EUR 126
Description: STAT5 Inhibitor is a cell-permeable inhibitor of STAT5 with IC50 value of 47 ?M against STAT5? SH2 domain EPO peptide binding activity [1].

CBF? Inhibitor

C3398-10 10 mg
EUR 203
Description: CBF? inhibitor is a small molecule which binds to CBF? and inhibits its association with Runx1 [1].Core binding factors (CBFs) are heterodimeric transcription factors containing a DNA-binding CBF? component (a RUNX protein) and an enhancer of binding, CBF?.

EGFR Inhibitor

C3327-1 1 mg
EUR 154
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family.

EGFR Inhibitor

C3327-25 25 mg
EUR 1146
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family.

EGFR Inhibitor

C3327-5 5 mg
EUR 363
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family.

CBF? Inhibitor

C3398-25 25 mg
EUR 393
Description: CBF? inhibitor is a small molecule which binds to CBF? and inhibits its association with Runx1 [1].Core binding factors (CBFs) are heterodimeric transcription factors containing a DNA-binding CBF? component (a RUNX protein) and an enhancer of binding, CBF?.

CBF? Inhibitor

C3398-5 5 mg
EUR 131
Description: CBF? inhibitor is a small molecule which binds to CBF? and inhibits its association with Runx1 [1].Core binding factors (CBFs) are heterodimeric transcription factors containing a DNA-binding CBF? component (a RUNX protein) and an enhancer of binding, CBF?.

CDK4 inhibitor

B1233-10 10 mg
EUR 469
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

CDK4 inhibitor

B1233-100 100 mg
EUR 1592
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

CDK4 inhibitor

B1233-50 50 mg
EUR 1041
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

Endotoxin Inhibitor

H-1382.0001 1.0mg
EUR 113
Description: Sum Formula: C55H97N15O12S2; CAS# [147396-10-9]

Endotoxin Inhibitor

H-1382.0005 5.0mg
EUR 318
Description: Sum Formula: C55H97N15O12S2; CAS# [147396-10-9]

NFAT Inhibitor

H-4874.0500 0.5mg
EUR 273
Description: Sum Formula: C75H118N20O22S; CAS# [249537-73-3] net

NFAT Inhibitor

H-4874.1000 1.0mg
EUR 454
Description: Sum Formula: C75H118N20O22S; CAS# [249537-73-3] net

NFAT Inhibitor

A4539-1 1 mg
EUR 138
Description: Selective inhibitor of calcineurin-mediated dephosphorylation of nuclear factor of activated T cells (NFAT). Does not disrupt other calcineurin-dependent pathways. Inhibits NFAT activation and NFAT-dependent expression of endogenous cytokine genes in T cells.

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