11723 Results for: "Enzo Life Sciences"
cis-5,8,11-Eicosatrienoic acid ≥97% (by HPLC), colourless oil
Supplier: Enzo Life Sciences
Immunomodulatory and anti-inflammatory effects.
Expand 2 Items
SB239063 ≥97% (by HPLC)
Supplier: Enzo Life Sciences
A potent, cell permeable inhibitor of p38 MAP kinase (IC50=44nM for recombinant purified human p38α). Inhibits IL-1 and TNF-α production in LPS-stimulated human peripheral blood monocytes (IC50=120nM and 350nM, respectively). Reported to protect against mild excitotoxic neuronal injury caused by NMDA and provides substantial protection against cell death induced by either oxygen glucose deprivation (OGD) or magnesium deprivation in cultured neurons. Also, reduces myocardial reperfusion injury via inhibition of endothelial adhesion molecule expression and blockade of polymorphonuclear (PMN) accumulation.
Expand 3 Items
Anti-HMOX1 Rabbit Polyclonal Antibody
Supplier: Enzo Life Sciences
Heme Oxygenase-1 (HO-1) also known as Hsp32, is the inducible isoform of heme oxygenase that catalyzes the NADPH, oxygen, and cytochrome P450 reductase dependent oxidation of heme to carbon monoxide, ferrous iron and biliverdin which is rapidly reduced to bilirubin.
Expand 4 Items

Why Choose Corning Fetal Bovine Serum?
Our vertically integrated FBS serum supply chain, from collection to scientist, allows us to provide a consistent supply of FBS.
PBS (endotoxin-free), Enzo Life Sciences
Supplier: Enzo Life Sciences
Sterile and endotoxin-free PBS for use with TLRgrade™ or endotoxin-free grade reagents.
Expand 4 Items
Sodium chloride 0.9% physiological saline endotoxin-free, sterile
Supplier: Enzo Life Sciences
Sterile and endotoxin-free physiological saline for use with TLRgrade™ or endotoxin-free grade reagents.
Expand 1 Items
(+/-)-Anatoxin ≥98% (by TLC)
Supplier: Enzo Life Sciences
Nicotinic acetylcholine receptor ligand.
Expand 1 Items
Human recombinant Calnexin (lumenal domain) (from E. coli)
Supplier: Enzo Life Sciences
Produced in E. coli.
Expand 4 Items
H₂S Donor 5a ≥98%, white solid
Supplier: Enzo Life Sciences
Cysteine-activated H2S donor. Stable in aqueous buffers. Does not react with potential cellular nucleophiles such as -OH and -NH₂ groups.
Expand 1 Items
GABAergic ligand library, Screen-Well®
Supplier: Enzo Life Sciences
The GABAergic igands library contains 56 ligands including endogenous neurotransmitters, agonists, antagonists, and marketed drugs. The library is ideal for screening or identifying recombinant orphan G protein-coupled receptors, target validation, secondary screening, assay development, and other pharmacological applications. The GABAergics ligands plate is 1 plate of the larger neurotransmitter library which contains over 650 CNS receptor ligands.
Expand 4 Items
Fatty acid library plates, SCREEN-WELL®
Supplier: Enzo Life Sciences
SCREEN-WELL® Fatty Acid Library contains 64 fatty acids of varying saturation and chain length.
Expand 4 Items
Kinase inhibitor library, Screen-Well®
Supplier: Enzo Life Sciences
The Screen-Well™ Kinase Inhibitor Library contains 80 known kinase inhibitors of well-defined activity. Inhibitors are supplied dissolved in DMSO at 10 mM and aliquoted into deep-well plates at either 100 or 500 ml per well. The library is an ideal tool for chemical genomics, assay development and other pharmacological applications. Includes inhibitors of these important kinases: Insulin/IGF Receptors, PI 3-Kinase, CaM Kinase II, JAK, PKA, CDK, JNK, PKC, CKI II, MAPK, RAF, EGFR, MEK, SAPK, GSK, MLCK, Src-family, IKK, PDGFR, VEGFR and many more.
Expand 4 Items
Metabotropic glutamatergic ligand library, Screen-Well®
Supplier: Enzo Life Sciences
The Screen-Well® metabotropic glutamatergic ligands plate contains 49 ligands including endogenous neurotransmitters, agonists, antagonists, and marketed drugs. The library is ideal for screening or identifying recombinant orphan G protein coupled receptors, target validation, secondary screening, assay development, and other pharmacological applications. The metabotropic glutamatergic ligands plate is 1 plate of the larger neurotransmitter library which contains over 650 ligands.
Expand 4 Items
Opioid ligand library, Screen-Well®
Supplier: Enzo Life Sciences
The Screen-Well® opioid and sigma ligands plate contains 74 ligands including endogenous neurotransmitters, agonists, antagonists, and marketed drugs. The library is ideal for screening or identifying recombinant orphan G protein coupled receptors, target validation, secondary screening, assay development, and other pharmacological applications. The opioid and sigma ligands plate is 1 plate of the larger Neurotransmitter Library which contains over 650 ligands.
Expand 4 Items
Cholinergic ligand library, Screen-Well®
Supplier: Enzo Life Sciences
The cholinergic ligands plate contains 72 compounds ligands including endogenous neurotransmitters, agonists, antagonists, and marketed drugs. The library is ideal for screening or identifying recombinant orphan G protein coupled receptors, target validation, secondary screening, assay development, and other pharmacological applications. The cholinergic ligands plate is 1 plate of the larger neurotransmitter library which contains over 650 ligands.
Expand 4 Items
Curvularin ≥95% (by HPLC)
Supplier: Enzo Life Sciences
Inhibitor of iNOS expression
Expand 2 Items
AG-494 ≥98% (by TLC)
Supplier: Enzo Life Sciences
AG-494 is a member of the tyrphostin family of tyrosine kinase inhibitors and is a potent inhibitor of EGF receptor autophosphorylation (IC50=1.2 µM) and EGF-dependent cell growth (IC50=6 µM). It selectively inhibits HER1 (EGF receptor) vs. HER1-2 receptor autophosphorylation (HER1: IC50=1.1 µM; HER1-2: IC50=45 µM). HER1-2 is a chimeric receptor consisting of the external HER1 domain fused to an internal HER2 domain. Blocks CDK2 activation and causescells to arrest at late G1 and during S phase.
Expand 1 Items
Herbimycin A ≥98% (by HPLC)
Supplier: Enzo Life Sciences
Antibiotic. Cell permeable tyrosine kinase inhibitor. It is effective on Src, Yes, Fps, Ros, Abl and ErbB oncogene products and inhibits thrombin-induced tyrosine phosphorylation of phospholipase C. It also inhibits HSP90, NF-κB activation and angiogenesis. Increases the sensitivity of certain cancer cells to chemotherapeutic agents. Blocks mitotic activity. Neurotoxic.
Expand 2 Items
Cycloheximide ≥95% (by TLC)
Supplier: Enzo Life Sciences
Protein synthesis inhibitor
Expand 2 Items
Vancomycin hydrochloride (from Streptomyces lysosup)
Supplier: Enzo Life Sciences
Glycopeptide antibiotic. Interferes with cell wall synthesis. Effective against Gram-positive bacteria.
Expand 2 Items
MMP inhibitor profiling kit
Supplier: Enzo Life Sciences
The MMP inhibitor profiling kit, fluorometric RED is a complete assay system designed to examine the specificity of inhibitors against a panel of ten matrix metalloproteinase enzymes, using a quenched fluorogenic substrate OMNIMMP® RED.
Expand 2 Items
Human recombinant TARC
Supplier: Enzo Life Sciences
Produced in E. coli. Non-glycosylated protein, containing 71 amino acids.
Expand 3 Items
Human recombinant IL-6
Supplier: Enzo Life Sciences
Produced in E. coli. Non-glycosylated protein, containing 184 amino acids.
Expand 2 Items
Tyrphostin AG 490 ≥98% (by TLC)
Supplier: Enzo Life Sciences
AG-490 is a potent inhibitor of the JAK-2 tyrosine kinase. In acute lymphoblastic leukemia (ALL) cells, which abundantly express JAK-2, AG-490 dose-dependently inhibited DNA synthesis, blocked cell growth and induced apoptosis. At 5 µM, AG-490 almost completely blocked the growth of all pre-B ALL cells but had no significant effect on the growth of mitogen-stimulated normal B or T cells, B-cell lymphoma or T-cell leukemia cells. AG-490 does not significantly inhibit other kinases such as Lck, Lyn, Btk, Syk and Src. It blocks interleukin-7-induced JAK kinase activity in T-cells (JAK-1, JAK-3) and the consequent phosphorylation of PI-3 kinase. AG-490 is cell permeable and is a valuable tool for studying the cellular role of JAK kinases in signal transduction.
Expand 2 Items
HBDDE ≥95% (by TLC)
Supplier: Enzo Life Sciences
Inhibits PKCα (IC50=43 µM) and PKCγ (IC50=50 µM) without inhibiting the δ, βI and βII isotypes.