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Non-antibody Products (Kits, Proteins, Microbial Antigens, Tissues, Services, etc.) - Page 12 of 5,802
Page 12 of 5,802
Records 551 - 600 of 290,077
[1]  «  7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17  »  [5802]
Results per Page: 25 | 50 | 75 | 100
Name Description Size Catalog # Supplier  
AM251 CB1 receptor antagonist / inverse agonist 10mg Asc-088-10mg
ASCENT SCIENTIFIC LTD.		 More Info
AM251 CB1 receptor antagonist / inverse agonist 50mg Asc-088-50mg
ASCENT SCIENTIFIC LTD.		 More Info
AM404 Anandamide transport inhibitor 10mg Asc-095-10mg
ASCENT SCIENTIFIC LTD.		 More Info
AM404 Anandamide transport inhibitor 50mg Asc-095-50mg
ASCENT SCIENTIFIC LTD.		 More Info
AM 80 Minimum Purity: > 99%. Retinoic acid receptor alpha (RARalpha) agonist that induces differentiation (ED50 = 0.79 nM) and apoptosis of HL-60 cells in vitro. Exhibits antiproliferative effects against a variety of human tumor cells lines (mean value... 10mg 3507
TOCRIS BIOSCIENCE		 More Info
AM 80 Minimum Purity: > 99%. Retinoic acid receptor alpha (RARalpha) agonist that induces differentiation (ED50 = 0.79 nM) and apoptosis of HL-60 cells in vitro. Exhibits antiproliferative effects against a variety of human tumor cells lines (mean value... 50mg 3507
TOCRIS BIOSCIENCE		 More Info
AM 580 Minimum Purity: > 98%. An analog of retinoic acid that acts as a selective RARalpha agonist (EC50 values are 0.3, 8.6 and 13 nM for RARalpha, RARbeta and RARgamma respectively). Significantly induces IL-4, IL-5 and IL-13 and inhibits IL-12 and IFN... 10mg 760
TOCRIS BIOSCIENCE		 More Info
AM 580 Minimum Purity: > 98%. An analog of retinoic acid that acts as a selective RARalpha agonist (EC50 values are 0.3, 8.6 and 13 nM for RARalpha, RARbeta and RARgamma respectively). Significantly induces IL-4, IL-5 and IL-13 and inhibits IL-12 and IFN... 50mg 760
TOCRIS BIOSCIENCE		 More Info
AM 630 Minimum Purity: > 98%. CB2 antagonist/inverse agonist (Ki = 31.2 nM) that displays 165-fold selectivity over CB1 receptors. Behaves as a weak partial/inverse agonist at CB1 receptors. 10mg 1120
TOCRIS BIOSCIENCE		 More Info
AM 630 Minimum Purity: > 98%. CB2 antagonist/inverse agonist (Ki = 31.2 nM) that displays 165-fold selectivity over CB1 receptors. Behaves as a weak partial/inverse agonist at CB1 receptors. 50mg 1120
TOCRIS BIOSCIENCE		 More Info
AM 251 Minimum Purity: > 99%. Potent CB1 receptor antagonist (IC50 = 8 nM, Ki = 7.49 nM) that displays 306-fold selectivity over CB2 receptors. Also potent GPR55 agonist (EC50 = 39 nM). Also available as part of the Cannabinoid CB1 Receptor Tocriset&trad... 10mg 1117
TOCRIS BIOSCIENCE		 More Info
AM 251 Minimum Purity: > 99%. Potent CB1 receptor antagonist (IC50 = 8 nM, Ki = 7.49 nM) that displays 306-fold selectivity over CB2 receptors. Also potent GPR55 agonist (EC50 = 39 nM). Also available as part of the Cannabinoid CB1 Receptor Tocriset&trad... 50mg 1117
TOCRIS BIOSCIENCE		 More Info
AM 251 Minimum Purity: > 99%. Potent CB1 receptor antagonist (IC50 = 8 nM, Ki = 7.49 nM) that displays 306-fold selectivity over CB2 receptors. Also potent GPR55 agonist (EC50 = 39 nM). Also available as part of the Cannabinoid CB1 Receptor Tocriset&trad... 1mg 1117
TOCRIS BIOSCIENCE		 More Info
AM 404 Minimum Purity: > 98%. Competitive and selective inhibitor of carrier-mediated anandamide transport (IC50 = 1 µM). Does not activate CB1 receptors or inhibit anandamide hydrolysis but has been shown to activate native and cloned vanilloid re... 10mg 1116
TOCRIS BIOSCIENCE		 More Info
AM 404 Minimum Purity: > 98%. Competitive and selective inhibitor of carrier-mediated anandamide transport (IC50 = 1 µM). Does not activate CB1 receptors or inhibit anandamide hydrolysis but has been shown to activate native and cloned vanilloid re... 50mg 1116
TOCRIS BIOSCIENCE		 More Info
AM 281 Minimum Purity: > 99%. Potent, selective CB1 cannabinoid receptor antagonist/inverse agonist (Ki values are 12 and 4200 nM for CB1 and CB2 receptors respectively). Increases locomotor activity following systemic administration in vivo. Analog of S... 10mg 1115
TOCRIS BIOSCIENCE		 More Info
AM 281 Minimum Purity: > 99%. Potent, selective CB1 cannabinoid receptor antagonist/inverse agonist (Ki values are 12 and 4200 nM for CB1 and CB2 receptors respectively). Increases locomotor activity following systemic administration in vivo. Analog of S... 50mg 1115
TOCRIS BIOSCIENCE		 More Info
AM 1172 Minimum Purity: > 98%. Metabolically stable anandamide uptake inhibitor (IC50 = 2.1 - 2.5 µM) and fatty acid amide hydrolase (FAAH) inhibitor (Ki = 3.18 µM). Inhibits N-arachidonylethanolamine (AEA) accumulation (IC50 = 24 µM) an... 10mg 3381
TOCRIS BIOSCIENCE		 More Info
AM 114 Minimum Purity: > 98%. Inhibitor of the chymotrypsin-like activity of the 20S proteasome (IC50 ~ 1 µM). Displays anticancer activity; inhibits cell growth in human colon cancer HCT116 p53+/+ cells (IC50 = 1.49 µM). 10mg 2564
TOCRIS BIOSCIENCE		 More Info
AM 114 Minimum Purity: > 98%. Inhibitor of the chymotrypsin-like activity of the 20S proteasome (IC50 ~ 1 µM). Displays anticancer activity; inhibits cell growth in human colon cancer HCT116 p53+/+ cells (IC50 = 1.49 µM). 50mg 2564
TOCRIS BIOSCIENCE		 More Info
AM 114 Proteasome Inhibitor 10 mg 2564/10
R&D SYSTEMS, INC.		 More Info
AM 114 Proteasome Inhibitor 50 mg 2564/50
R&D SYSTEMS, INC.		 More Info
AM 1172 Cannabinoid Transporter Inhibitor 10 mg 3381/10
R&D SYSTEMS, INC.		 More Info
AM 251 Cannabinoid R1/CB1 Antagonist 1 mg 1117/1
R&D SYSTEMS, INC.		 More Info
AM 251 Cannabinoid R1/CB1 Antagonist 10 mg 1117/10
R&D SYSTEMS, INC.		 More Info
AM 251 Cannabinoid R1/CB1 Antagonist 50 mg 1117/50
R&D SYSTEMS, INC.		 More Info
AM 281 Cannabinoid R1/CB1 Antagonist 10 mg 1115/10
R&D SYSTEMS, INC.		 More Info
AM 281 Cannabinoid R1/CB1 Antagonist 50 mg 1115/50
R&D SYSTEMS, INC.		 More Info
AM 404 Cannabinoid Transporter Inhibitor 10 mg 1116/10
R&D SYSTEMS, INC.		 More Info
AM 404 Cannabinoid Transporter Inhibitor 50 mg 1116/50
R&D SYSTEMS, INC.		 More Info
AM 580 Retinoic Acid Receptor Agonist 10 mg 0760/10
R&D SYSTEMS, INC.		 More Info
AM 580 Retinoic Acid Receptor Agonist 50 mg 0760/50
R&D SYSTEMS, INC.		 More Info
AM 630 Cannabinoid R2/CB2 Antagonist 10 mg 1120/10
R&D SYSTEMS, INC.		 More Info
AM 630 Cannabinoid R2/CB2 Antagonist 50 mg 1120/50
R&D SYSTEMS, INC.		 More Info
AM 80 Retinoic Acid Receptor Agonist 10 mg 3507/10
R&D SYSTEMS, INC.		 More Info
AM 80 Retinoic Acid Receptor Agonist 50 mg 3507/50
R&D SYSTEMS, INC.		 More Info
Amanitin 1 mg; from Amanita phalloides. Formula: C39H54N10O14SLD50: approximately 0.1 mg/kg (oral, man)Molecular weight: Mr = 919. Bicyclic octapeptide that inhibits the RNA polymerase of eukaryotic cells. n/a 10161284001 ROCHE APPLIED SCIENCE More Info
alpha-Amanitin Minimum Purity: > 95%. Inhibitor of RNA polymerase II. Inhibits transcription in eukaryotic cells. Binds and blocks the largest subunits of RNA polymerase II, preventing new ribonucleotides from incorporating into the nascent RNA chain. Potent ama... 1mg 4025
TOCRIS BIOSCIENCE		 More Info
alpha-Amanitin RNA/DNA Polymerase Inhibitor 1 mg 4025/1
R&D SYSTEMS, INC.		 More Info
AMG 9810 Minimum Purity: > 98%. Potent and selective, competitive vanilloid TRPV1 receptor antagonist (IC50 = 17 nM). Inhibits capsaicin-, proton-, heat- and endogenous ligand-induced activation of human and rat recombinant TRPV1 receptors. Displays antihy... 10mg 2316
TOCRIS BIOSCIENCE		 More Info
AMG 9810 Minimum Purity: > 98%. Potent and selective, competitive vanilloid TRPV1 receptor antagonist (IC50 = 17 nM). Inhibits capsaicin-, proton-, heat- and endogenous ligand-induced activation of human and rat recombinant TRPV1 receptors. Displays antihy... 50mg 2316
TOCRIS BIOSCIENCE		 More Info
AMG-073 AMG-073(Cinacalcet hydrochloride) represents a new class of compounds for the treatment of hyperparathyroidism. Purity is greater than 99%. 10 mg orb60063
BIORBYT LTD.		 More Info
AMG-208 AMG 208 is a small molecule inhibitor of c-Met with an IC50 of 9.3 nM. Purity is greater than 99%. 10 mg orb60318
BIORBYT LTD.		 More Info
AMG 9810 TRPV Antagonist 10 mg 2316/10
R&D SYSTEMS, INC.		 More Info
AMG 9810 TRPV Antagonist 50 mg 2316/50
R&D SYSTEMS, INC.		 More Info
AMI-193 Minimum Purity: > 99%. Selective 5-HT antagonist, which binds to 5-HT2 sites as potently as spiperone but has lower affinity for 5-HT2C receptors. Also a high affinity D2 receptor antagonist (Ki = 3 nM). Lacks the disruptive effect of spiperone on... 10mg 524
TOCRIS BIOSCIENCE		 More Info
AMI-193 Minimum Purity: > 99%. Selective 5-HT antagonist, which binds to 5-HT2 sites as potently as spiperone but has lower affinity for 5-HT2C receptors. Also a high affinity D2 receptor antagonist (Ki = 3 nM). Lacks the disruptive effect of spiperone on... 50mg 524
TOCRIS BIOSCIENCE		 More Info
AMI-1 Cell-permeable. A potent and specific protein arginine N-methyltransferase (PRMTs) inhibitor (IC50 = 8.8 µM for human PRMT1 and 3.0 µM for yeast Hmt1p ). Does not compete for the AdoMet (S-adenosyl-L-methionine; SAM) binding site. Also... 5 mg 1943-5
BIOVISION, INC.		 More Info
AMI-1 Cell-permeable. A potent and specific protein arginine N-methyltransferase (PRMTs) inhibitor (IC50 = 8.8 µM for human PRMT1 and 3.0 µM for yeast Hmt1p ). Does not compete for the AdoMet (S-adenosyl-L-methionine; SAM) binding site. Also... 25 mg 1943-25
BIOVISION, INC.		 More Info
AMI-193 Non-selective Dopamine Receptor Antagonist 10 mg 0524/10
R&D SYSTEMS, INC.		 More Info
Page 12 of 5,802
Records 551 - 600 of 290,077
[1]  «  7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17  »  [5802]
Results per Page: 25 | 50 | 75 | 100
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