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

BRAF inhibitor

A3263-10 10 mg
EUR 459.6
Description: BRAF inhibitor is a potent BRAF inhibitor.

BRAF inhibitor

A3263-5.1 10 mM (in 1mL DMSO)
EUR 537.6
Description: BRAF inhibitor is a potent BRAF inhibitor.

BRAF inhibitor

A3263-50 50 mg
EUR 1182
Description: BRAF inhibitor is a potent BRAF inhibitor.

CDK9 inhibitor

A3294-10 10 mg
EUR 393.6
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes.

CDK9 inhibitor

A3294-100 100 mg
EUR 1796.4
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes.

CDK9 inhibitor

A3294-5 5 mg
EUR 236.4
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes.

CDK9 inhibitor

A3294-5.1 10 mM (in 1mL DMSO)
EUR 254.4
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes.

CDK9 inhibitor

A3294-50 50 mg
EUR 1015.2
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes.

ITK inhibitor

A3509-10 10 mg
EUR 927.6
Description: Interleukin-2-inducible T cell kinase (ITK) is a non-receptor tyrosine kinase expressed in T cells, NKT cells and mast cells which plays a crucial role in regulating the T cell receptor (TCR), CD28, CD2, chemokine receptor CXCR4, and FcepsilonR-mediated signaling pathways.

ITK inhibitor

A3509-50 50 mg
EUR 2448
Description: Interleukin-2-inducible T cell kinase (ITK) is a non-receptor tyrosine kinase expressed in T cells, NKT cells and mast cells which plays a crucial role in regulating the T cell receptor (TCR), CD28, CD2, chemokine receptor CXCR4, and FcepsilonR-mediated signaling pathways.

Rinbonuclease Inhibitor

abx098030-10kU 10 kU
EUR 644.4

Rinbonuclease Inhibitor

abx098030-2kU 2 kU
EUR 510

NFAT Inhibitor

A4539-1 1 mg
EUR 165.6
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.

NFAT Inhibitor

A4539-10 10 mg
EUR 915.6
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.

NFAT Inhibitor

A4539-5 5 mg
EUR 540
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.

Elastase Inhibitor

A2579-5 5 mg
EUR 199.2
Description: A potent, irreversible inhibitor of human neutrophil elastase (HNE). The structure of the enzyme-inhibitor complex reveals crosslinking of the catalytic residues His-57 and Ser-195 by the peptidyl chloromethylketone.

Apoptosis Inhibitor

A1930-10 10 mg
EUR 170.4
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay.

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