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Supplier: Enzo Life Sciences
Description: A cell permeable, highly specific, potent and ATP-competitive inhibitor of Rho kinase (ROCK) (Ki=1.6nM). Exhibits a much weaker affinity for other serine/threonine kinases (Ki=630nM for PKA, 9.27mM for PKC and 10.1mM for MLCK). More potent and selective than Y-27632. Inhibits the phosphorylation of MARCKS in cells stimulated by lysophosphatidic acid. Inhibits EP3-stimulated NO formation. Prevents fragmentation of apoptotic cells. Relieves neuropathic pain.

Supplier: Enzo Life Sciences
Description: Useful negative control for the PI(3)K (phosphoinositide 3-kinase) inhibitor LY-294,002. Does not inhibit PI(3)K even at concentrations

Supplier: Enzo Life Sciences
Description: Highly potent and selective ETB-receptor antagonist.

Supplier: Enzo Life Sciences
Description: Neuropeptide

Catalog Number: (89154-122)
Supplier: Enzo Life Sciences
Description: Host: Mouse, Isotype: IgG1


Catalog Number: (89154-094)
Supplier: Enzo Life Sciences
Description: Host: Rat, Isotype: IgG2a


Catalog Number: (89154-140)
Supplier: Enzo Life Sciences
Description: Host: Mouse, Isotype: IgG1


Catalog Number: (89154-682)
Supplier: Enzo Life Sciences
Description: Host: Mouse, Isotype: IgG1


Catalog Number: (89154-650)
Supplier: Enzo Life Sciences
Description: Host: Rat, Isotype: IgG1


Catalog Number: (89144-066)
Supplier: Enzo Life Sciences
Description: Active form of SUMO-2


Catalog Number: (89143-988)
Supplier: Enzo Life Sciences
Description: Produced in E. coli.


Catalog Number: (89145-214)
Supplier: Enzo Life Sciences
Description: Host: Rabbit


Catalog Number: (89155-870)
Supplier: Enzo Life Sciences
Description: Kills Fas-sensitive cells at concentrations of >1ng/ml in the presence of cross-linking enhancer.


Catalog Number: (89154-910)
Supplier: Enzo Life Sciences
Description: Host: Rat, Isotype: IgG2a


Supplier: Enzo Life Sciences
Description: EGFR inhibitor

Catalog Number: (89158-360)
Supplier: Enzo Life Sciences
Description: Endogenous cannabinoid. Weak ligand of CB1 (Ki=23.8µM) and CB2 (Ki=13.9µM) receptor. Inhibits fatty acid amide hydrolase (FAAH) (IC50=5.1µM). Immunosuppressant, anti-inflammatory, anti-nociceptive and anti-convulsant in vivo. The exact mode of action has not yet been revealed. It has been suggested that PEA: i) binds to a yet to be discovered cannabinoid receptor similar to CB2; ii) administered in vivo elicits the synthesis of endogenous agonists of CB2; iii) acts as an "entourage" compound by enhancing the activity and/or by influencing the turnover of endogenous agonists of CB2, possibly but not uniquely, by inhibiting their degradation.


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
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