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Org Jade™ QRT Kit-iCycler | M1180

Org Jade™ QRT Kit-Low ROX | M1181

Org Jade™ QRT Kit-ROX | M1182

Org Taqman QRT Kit | M1187

Org Taqman QRT Kit-iCycler | M1188

Org Taqman QRT Kit-Low ROX | M1189

Org Taqman QRT Kit-ROX | M1190

K414 | OrgFrontier™ Plasma Membrane Isolation Kit DataSheet

Oridonin, a diterpenoid isolated from Rabdosia rubescens displays anti-inflammatory, anti-bacterial, anti-tumor effects and has been used for the treatment of human cancers, especially esophageal...

Oritavancin diphosphate is a second-generation, semi-synthetic lipoglycopeptide, that is derived from chloroeremomycin, an analogue of vancomycin. Similar to vancomycin, it contains a core...

Orlistat is a cell-permeable, selective, and competitive lipase inhibitor (IC₅₀ = 0.15 µM). Targets serine hydrolases in the nervous system, such as diacylglycerol lipase (DAGL), which is responsible...

K939 | Ornithine Assay Kit Fluorometric DataSheet

K176 | Ornithine Decarboxylase I ODC1 Inhibitor Screening Kit Colorimetric DataSheet

ODC is pyridoxal phosphate dependent amino acid deacarboxylase, which catalyzes the conversion of ornithine to putrescine. It is the first and rate-limiting step in the polyamine biosynthetic pathway...

ORY-1001 is a potent and selective inhibitor of LSD1 (IC₅₀ < 20 nM). It targets acute myeloid leukemia (AML) stem cells and significantly reduces tumor cell load while increasing survival time in...

Alpha 1 Antitrypsin is an acute-phase plasma protein found at 290 mg per 100 ml. It functions as a serine protease inhibitor with targets like elastase, plasmin, collagenase, thrombin, leucocyte...

Human epidermal growth factor, also known as EGF, is a 6kD protein with 53 amino acid residues and three intramolecular disulfide bonds. By binding with high affinity to epidermal growth fact...

Human basic fibroblast growth factor, also known as bFGF, FGF2 or FGF-, is a member of the fibroblast growth factor family. It is a single-chain polypeptide growth factor that plays a significant...

Fibronectin (rFn) is a high-molecular weight, a glycoprotein of the extracellular matrix. FN binds extracellular matrix components such as collagen, fibrin and heparan sulfate proteoglycans. FN...

Serum albumin, the main protein of plasma, has a good binding capacity for water, Ca2+, Na+, K+, fatty acids, hormones, bilirubin and drugs. Its main function is the regulation of the colloidal...

Human insulin-like growth factor-1 Long R3(IGF-1 LR3) are produced with the animal component free bioreactor. IGF-1 LR3(Long Arg3 IGF-1) is an 83 amino acid analog of IGF-1 comprising the complete...

Lactoferrin (LF), also known as lactotransferrin (LTF), is a globular glycoprotein with a molecular mass of about 80kD, which consists of two highly homologous lobes, designated the N and C lobes...

Lysozyme(LYZ) is a small protein with 14.7kDa molecular weight and a pl(isoelectric point) of 11.4, contains 129 amino acid. LYZ is a potent amtimicrobial enzyme, by catalytic hydrolysis of their...

Oseltamivir acid (GS-4071) is the active metabolite of oseltamivir (Cat. No. B1885). It acts as an inhibitor of influenza neuraminidases A and B (IC₅₀ = 0.1 to 4.9 nM for both enzymes), in this way...

Oseltamivir Phosphate is an antiviral prodrug targeted against the influenza viruses. Once hydrolyzed in the liver to its active metabolite, oseltamivir acid it competitively inhibits viral...

OSI-027 is a potent mammalian target of rapamycin (mTOR) kinase inhibitor with potential antineoplastic activity. It binds to and inhibits both the raptor-mTOR (TOR complex 1 or TORC1) and the...

OSI-420 is an active metabolite of Erlotinib (Cat. No. 1588) which is an orally active EGFR tyrosine kinase inhibitor with IC₅₀ of 2 and 20 nM for the inhibition of human EGFR and EGFR...

OSI-930 is a potent inhibitor of receptor tyrosine kinases with IC50 values of 80 nM, 9 nM, 8 nM, 15 nM, 41 nM and 22 nM for c-Kit, KDR, Flt, CSF-1R, c-Raf and Lck respectively.OSI-930 is a potent...

Osilodrostat is a potent inhibitor of the enzymes 11β-hydroxylase (CYP11B1) and aldosterone synthase (CYP11B2), which catalyze the final steps of cortisol and aldosterone biosynthesis, respectively,...

OSMI-1 is a potent, cell-permeable, O-GlcNAc transferase (OGT) inhibitor. inhibits protein O-GlcNAcylation in several mammalian cell lines without qualitatively altering cell surface N- or O-linked...

OSS-128167 is a potent and selective inhibitor of sirtuin 6 (SIRT6; IC50 = 89 μM). It displays selectivity for SIRT6 over SIRT1 and SIRT2 (IC50s = 1,578 and 751 μM, respectively). OSS-128167...

Osteopontin OPN human Elisa Kit | K7335

Osteopontin (OPN), also known as Secreted phosphoprotein 1 (SPP1), is a human gene product which is conserved in other species. This protein is glycoprotein that was first identified in osteoblasts...

Human OPG (Osteoprotegerin), also known as OCIF (Osteoclastogenesis inhibitory factor), is a member of the TNF receptor superfamily. Recombinant human OPG/OCIF specifically acts on bone tissues and...

Osteoclast-stimulating factor-1 (OSTF1) is an intracellular protein produced by osteoclasts that indirectly induces osteoclast (OCL) formation and bone resorption. OSTF1 is highly expressed in OCL...

A novel celecoxib derivative, that acts as a potent inhibitor of 3-phosphoinositide-dependent kinase-1 (PDK1) activity (IC₅₀ = 5 µM for recombinant PDK1). It displays anti-cancer activity in a...

Otenabant is a novel cannabinoid type 1 (CB1) receptor antagonist. It is effective at subnanomolar concentrations at human CB1 receptors in binding and functional assays, with Ki values of 0.7 nM and...

TOR proteins is also known as fibrocyte-derived protein (Fdp) and Melanoma inhibitory activity-like (MIAL). Otoraplin is a member of the melanoma-inhibiting activity gene family. Otoraplin is a...

OTS-964 is a potent inhibitor of lymphokine-activated killer T cell-originated protein kinase (TOPK; IC₅₀ = 28 nM). It specifically blocks cytokinesis, leading to apoptosis, in a broad range of...

OTSSP167 is an inhibitor (IC₅₀ = 0.41 nM) of maternal embryonic leucine zipper kinase (MELK) with potential antineoplastic activity. OTSSP167 binds to MELK, which prevents both MELK phosphorylation...

OTX015 is a potent inhibitor of BRD2, BRD3, and BRD4 (EC₅₀s = 10-19 nM). It displays antiproliferative effects at a sub-micromolar range in vitro in a wide range of solid tumor types and leukemias,...

3918 | OTX1 Antibody DataSheet

Ouabain is a cardioactive glycoside consisting of rhamnose and ouabagenin, obtained from the seeds of Strophanthus gratus and other plants of the Apocynaceae. Acts as a potent and selective Na⁺/K⁺...

Outstretched DNA Polymerase | M1152

E4358 | Ovalbumin OVA Human Elisa Kit DataSheet

Ovarian tumor suppressor candidate 2, also known as OVCA2, belongs to the uPF0483 family. It is ubiquitously expressed and produces proteins that help repair damaged DNA and slows cell division. Its...

3890 | OX40 Antibody DataSheet

3890BP | OX40 Blocking Peptide DataSheetAntibody Target: OX40 Accession #: NP_037181Gene ID: 25572Appearance: Colorless liquidConcentration: 0.5 mg/mlFormulation: 50 µg (0.5 mg/ml) in phosphate...

K4174 | OX40 Ligand / TNFSF4 Human Elisa Kit DataSheet

K4173 | OX40/CD134 Human Elisa Kit DataSheet

OXA-01 is an ATP-competitive, selective dual inhibitor of mTORC1/mTORC2. Displays antiangiogenic and antitumor properties.OXA-01 is an ATP-competitive, selective dual inhibitor of mTORC1/mTORC2...

K664 | Oxalate Decarboxylase Activity Colorimetric Assay Kit DataSheet

Oxalate decarboxylase (OxdC, EC4.1.1.2) is a manganese-containing enzyme, which decomposes oxalic acid and oxalate. With OxdC catalysis, oxalate is split into formate and CO2. This enzyme belongs to...

K663 | Oxalate Oxalic Acid Colorimetric Assay Kit DataSheet

K509 | Oxalate Oxidase Activity Assay Kit Fluorometric DataSheet

Oxaliplatin is a third-generation, diaminocyclohexane-containing platinum anti-cancer drug. The anticancer activity and the antitumor specificity of oxaliplatin mainly depend on human organic cation...

K659 | Oxaloacetate Colorimetric/Fluorometric Assay Kit DataSheet

A potent inhibitor of mammalian histone deacetylases (HDACs) (IC₅₀ = 15.7 nM). A novel antitumor agent; oxamflatin modifies epigenetic status and gene expression, increases blastocyst quality, and...

6672 | OxdC Antibody DataSheet

A broad spectrum benzimidazole anthelmintic. Mainly used for protecting livestock against roundworm, strongyles and pinworms. Oxfendazole is the sulfoxide metabolite of fenbendazole.A broad spectrum...

Hydrogen acceptor in the enzymatic determination of NADP and NADPH.Oxidized Glutathione is a hydrogen acceptor in the enzymatic determination of NADP and NADPH.1241 | Oxidized Glutathione (GSSG)...

OxiRed, which has been marketed under the name Amplex Red™ reagent, is a highly sensitive and stable probe for H₂O₂, is a fluorogenic (EX/EM = 535/587 nm) and Colorometric (l = 570 nm) substrate for...

E4516 | OxLDL Human Elisa Kit DataSheet

E4517 | OxLDL Mouse Elisa Kit DataSheet

E4518 | OxLDL Rat Elisa Kit DataSheet

Oxytetracycline is a tetracycline analog isolated from the actinomycete Streptomyces rimosus. It is an antibiotic used for treatment of infections caused by Gram positive and Gram negative...

Oxythiamine is a thiamine antagonist that acts as a transketolase inhibitor. As transketolase is a crucial enzyme of the pentose phosphate pathway, inhibition of this enzyme causes suppression of the...

Ozanimod (RPC1063) is an orally bioavailable agonist of the sphingosine-1-phosphate receptor subtypes 1 (S1P1) and 5 (S1P5). S1P receptors belong to the family of G-protein-coupled receptor which...

6970 | P-glycoprotein Antibody DataSheet

p-nitro-Pifithrin-α is a cell-permeable analog of pifithrin-α. Pifithrin-α is an inhibitor of p53 that blocks p53-dependent apoptosis. p-nitro-Pifithrin-α blocks p53-mediated expression of p21/WAF1...

3633R | P-Selectin Antibody DataSheet

3633RBP | P-Selectin Blocking Peptide DataSheetAntibody Target: P-SelectinAccession #: 6401Gene ID: 20344Appearance: Colorless liquidConcentration: 0.5 mg/mlFormulation: 50 µg (0.5 mg/ml) in...

P1,P5-di(adenosine-5′)-pentaphosphate ammonium salt is a potent inhibitor of heat shock protein 78 in Leishmania donovani (LdHSP78). LdHSP78 is a putative ClpB protease, that is important for...

p130Cas/BCAR1 is a member of the Cas family (Crk-associated substrate) of adaptor proteins and plays a central coordinating role for tyrosine kinase-based signaling related to cell adhesion. It is...

K346 | p300 Inhibitor Screening Assay Kit Fluorometric DataSheet

p38- is a member of the p38 MAP kinase family and is activated by both proinflammatory cytokines and environmental stress (1). The p38- is activated through its phosphorylation by MAP kinase kinases...

3114 | p38 MAP Kinase Antibody DataSheet

3114BP | p38 MAP Kinase Blocking Peptide DataSheetAntibody Target: p38 MAP Kinase Accession #: ACI00233Gene ID: 1432Appearance: Colorless liquidConcentration: 0.5 mg/mlFormulation: 50 µg (0.2 mg/ml)...

p38a (SAPK2A) is a member of the p38 MAPK family which are activated by various environmental stresses and proinflammatory cytokines (1). The activation of p38 requires its phosphorylation by MAP...

Mitogen-activated protein kinase (MAPK) cascades represent one of the major signal systems used by eukaryotic cells to transduce extracellular signals into cellular responses, and involved in a wide...

3542 | p42/44 MAPK Antibody DataSheet

3085R | p44/42 MAPK (Erk1/2) Antibody DataSheet

3085RBP | P44/p42 MAPK (Erk1/2) Blocking Peptide DataSheetAntibody Target: P44/p42 MAPK (Erk1/2)Accession #: P63086.3Gene ID: 116590Appearance: Colorless liquidConcentration: 0.5 mg/mlFormulation: 50...

P505-15 is a potent, cell-permeable, highly selective, small molecule SYK inhibitor (IC₅₀ = 1 nM) with anti-SYK activity that is at least 80-fold greater than its affinity for other kinases. P505-15...

Cell-permeable. A Selective inhibitor of the ubiquitin-specific protease USP7 (IC₅₀ = 4.2 µM). Induces apoptosis in multiple myeloma cells and overcomes bortezomib resistance. Displays antiangiogenic...

A potent PI3K/Akt/mTOR inhibitor that inhibits the TORC1 and TORC2 complexes. Displays inhibition of both Akt signaling and mTOR signaling similarly in tumor and vasculature. P529 inhibits tumor...

3036RBP | p53 Blocking Peptide DataSheetAntibody Target: p53 Accession #: EAW90140Gene ID: 7157Appearance: Colorless liquidConcentration: 0.5 mg/mlFormulation: 50 µg (0.5 mg/ml) in phosphate buffered...

K4829 | p53 human Elisa Kit DataSheet

p53 Mutant human recombinant | 4832

K961 | p53 Nuclear Translocation Assay Kit Cell-Based DataSheet

K923 | p53 Transcription Factor Activity Assay Kit DataSheet

3340 | p53DINP1 Antibody DataSheet

3340BP | p53DINP1 Blocking Peptide DataSheetAntibody Target: p53DINP1Accession #: Q96A56Gene ID: 94241Appearance: Colorless liquidConcentration: 0.5 mg/mlFormulation: 50 µg (0.5 mg/ml) in phosphate...

3295 | p53R2 Polyclonal Antibody DataSheet

3485 | p70 S6 Kinase Antibody DataSheet

Activation of cell growth leads to the multiple phosphorylation of 40S ribosomal protein S6. The kinase responsible for controlling this event is termed p70S6K (1). Northern blot analysis shows...

P7C3 is an aminopropyl carbazole derivative that acts as a proneurogenic, neuroprotective compound. Protects newborn neurons in the dentate gyrus by mitigating cell death. Also enhances learning and...

P7C3-A20 is a derivative of P7C3 (Cat. No. 2849), and is a proneurogenic, neuroprotective agent. P7C3-A20 displays increased activity and an improved toxicity profile compared to P7C3...

Procaspase-activating compound 1 (PAC-1) directly activates procaspase-3 to caspase-3, a transformation that allows induction of apoptosis even in cells that have defective apoptotic machinery. In...

PACAP (6-38) is a potent and competitive pituitary adenylate cyclase-activating polypeptide receptor (PAC)1 antagonist (IC₅₀ = 2 nM). Inhibits PACAP (1-27)-induced stimulation of adenylate cyclase...