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Non-antibody Products (Kits, Proteins, Microbial Antigens, Tissues, Services, etc.) - Page 4 of 5,777
Page 4 of 5,777
Records 151 - 200 of 288,813
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Name Description Size Catalog # Supplier  
ABT 751 Minimum Purity: > 98%. Antimitotic agent, inhibits microtubule polymerization. Binds to beta-tubulin on the colchine site; blocks cell cycle at G2M phase and induces apoptosis. Exhibits antitumor activity. Also displays activity in cell lines resi... 10mg 4138
TOCRIS BIOSCIENCE		 More Info
ABT-263 Bcl2 Family Inhibitor. Ki's of <1 nmol/L for Bcl2, Bcl-xL, and Bcl-w. Purity is greater than 99%. 5 mg orb60064
BIORBYT LTD.		 More Info
ABT-492 ABT-492 is a new fluoroquinolone against 155 aerobic and 171 anaerobic pathogens. Purity is greater than 99%. 10 mg orb60507
BIORBYT LTD.		 More Info
ABT-737 ABT-737 is a pan-Bcl2 inhibitor and ABT-737 single-agent LC90 values ranged from 100 nM for COG-LL-319. Purity is greater than 99%. 5 mg orb60030
BIORBYT LTD.		 More Info
ABT-751 ABT-751 is a novel bioavailable tubulin-binding and antimitotic sulfonamide agent with an IC50 of about 1.5 and 3.4 ?M in neuroblastoma and non-neuroblastoma cell lines. Purity is greater than 99%. 10 mg orb60192
BIORBYT LTD.		 More Info
ABT-869 ABT-869(Linifanib) is a structurally novel, potent RTK and VEGF and PDGF receptor families inhibitor with IC50 of 0.2, 2, 4, and 7 nM for human endothelial cells, PDGFR-beta, KDR, and CSF-1R, respectively. Purity is greater than 99%. 10 mg orb60065
BIORBYT LTD.		 More Info
ABT-888 ABT-888 is a potent inhibitor of both PARP-1 and PARP-2 by [3H]NAD+ with Kis of 5.2 and 2.9 nmol/L, respectively. Purity is greater than 99%. 5 mg orb60066
BIORBYT LTD.		 More Info
ABT-869 ABT-869 is multi-targeted inhibitor of all members of the VEGF and PDGF receptor families (e.g., KDR, IC50 value of 4 nM), but has much less activity (IC50 values >1 µM) against unrelated receptor tyrosine kinases, soluble tyrosine kinases o... 1 mg 1615-1
BIOVISION, INC.		 More Info
ABT-869 ABT-869 is multi-targeted inhibitor of all members of the VEGF and PDGF receptor families (e.g., KDR, IC50 value of 4 nM), but has much less activity (IC50 values >1 µM) against unrelated receptor tyrosine kinases, soluble tyrosine kinases o... 5 mg 1615-5
BIOVISION, INC.		 More Info
ABT-888 Potent inhibitor of PARP-1 and PARP-2 (potency ?5 nM in vitro). Does not inhibit other NAD-binding enzymes. Has minimal CYP450 inhibition and induction. Shows broad spectrum of chemo- and radio-potentiation. Does not show inherent cytotoxicity and... 1 mg 1620-1
BIOVISION, INC.		 More Info
ABT-888 Potent inhibitor of PARP-1 and PARP-2 (potency ?5 nM in vitro). Does not inhibit other NAD-binding enzymes. Has minimal CYP450 inhibition and induction. Shows broad spectrum of chemo- and radio-potentiation. Does not show inherent cytotoxicity and... 5 mg 1620-5
BIOVISION, INC.		 More Info
ABT 751 n/a 10 mg 4138/10
R&D SYSTEMS, INC.		 More Info
ABT 751 n/a 50 mg 4138/50
R&D SYSTEMS, INC.		 More Info
AC 264613 Minimum Purity: > 98%. Potent and selective protease-activated receptor 2 (PAR2) agonist (pEC50 = 7.5). Displays no activity at other PAR subtypes and exhibits no significant activity at over 30 other receptors implicated in nociception and inflam... 50mg 3370
TOCRIS BIOSCIENCE		 More Info
AC 264613 Minimum Purity: > 98%. Potent and selective protease-activated receptor 2 (PAR2) agonist (pEC50 = 7.5). Displays no activity at other PAR subtypes and exhibits no significant activity at over 30 other receptors implicated in nociception and inflam... 10mg 3370
TOCRIS BIOSCIENCE		 More Info
AC 45594 Minimum Purity: > 99%. Selective inverse agonist at the orphan nuclear receptor steroidogenic factor-1 (SF-1) (IC50= 50 - 100 nM). Displays no activity at estrogen, LRH-1, ROR, ERR or Nurr receptors. Inhibits SFRE-mediated transcription. 10mg 3043
TOCRIS BIOSCIENCE		 More Info
AC 45594 Minimum Purity: > 99%. Selective inverse agonist at the orphan nuclear receptor steroidogenic factor-1 (SF-1) (IC50= 50 - 100 nM). Displays no activity at estrogen, LRH-1, ROR, ERR or Nurr receptors. Inhibits SFRE-mediated transcription. 50mg 3043
TOCRIS BIOSCIENCE		 More Info
AC 187 Minimum Purity: > 98%. Orally active, potent amylin receptor antagonist (IC50 = 0.48 nM) that displays 38-fold and 400-fold selectivity over calcitonin and CGRP receptors respectively. Blocks amyloid beta-induced neurotoxicity by attenuating the a... 500µg 3419
TOCRIS BIOSCIENCE		 More Info
Ac2-26 Minimum Purity: > 98%. Annexin/lipocortin 1-mimetic peptide; inhibits leukocyte extravasation. Reduces neutrophil adhesion and emigration, and promotes detachment of neutrophils from activated mesenteric endothelium in mice in vivo. Anti-inflammat... 500µg 1845
TOCRIS BIOSCIENCE		 More Info
Ac2-12 Minimum Purity: > 98%. Annexin/lipocortin 1-mimetic peptide; inhibits leukocyte extravasation. Reduces neutrophil adhesion and emigration, and promotes detachment of neutrophils from activated mesenteric endothelium in mice in vivo. 1mg 1846
TOCRIS BIOSCIENCE		 More Info
Ac9-25 Minimum Purity: > 98%. N-terminal peptide of Annexin I (AI/Lipocortin I) that inhibits leukocyte extravasation. Acts as a formyl peptide receptor 1 (FPR1) ligand and stimulates neutrophil NADPH oxidase activation. 1mg 3231
TOCRIS BIOSCIENCE		 More Info
AC 55649 Minimum Purity: > 99%. Potent, isoform-selective RARbeta2 receptor agonist (pEC50 values are 6.9, 5.7 and 5.6 at RARbeta2, RARbeta1 and RARalpha respectively) that displays 100-fold selectivity versus other retinoid receptors. Inhibits proliferati... 10mg 2436
TOCRIS BIOSCIENCE		 More Info
AC 55649 Minimum Purity: > 99%. Potent, isoform-selective RARbeta2 receptor agonist (pEC50 values are 6.9, 5.7 and 5.6 at RARbeta2, RARbeta1 and RARalpha respectively) that displays 100-fold selectivity versus other retinoid receptors. Inhibits proliferati... 50mg 2436
TOCRIS BIOSCIENCE		 More Info
9-AC Minimum Purity: > 99%. Cl- transport inhibitor with a moderate to strong inhibitory action on PKA activated cardiac IcI. 100mg 963
TOCRIS BIOSCIENCE		 More Info
AC 261066 Minimum Purity: > 98%. Potent RARbeta2 agonist (pEC50 = 8.1). Selective over RARbeta1, RARalpha and RARgamma (pEC50 values are 6.4, 6.2 and 6.3 respectively). More potent and orally available than AC 55649 (Cat. No. 2436). 10mg 4046
TOCRIS BIOSCIENCE		 More Info
AC 261066 Minimum Purity: > 98%. Potent RARbeta2 agonist (pEC50 = 8.1). Selective over RARbeta1, RARalpha and RARgamma (pEC50 values are 6.4, 6.2 and 6.3 respectively). More potent and orally available than AC 55649 (Cat. No. 2436). 50mg 4046
TOCRIS BIOSCIENCE		 More Info
AC 55541 Minimum Purity: > 97%. Potent and selective protease-activated receptor 2 (PAR2) agonist (pEC50 = 6.7) that displays no activity at other PAR subtypes or at over 30 other receptors involved in nociception and inflammation. Stimulates cell prolifer... 10mg 3369
TOCRIS BIOSCIENCE		 More Info
AC 55541 Minimum Purity: > 97%. Potent and selective protease-activated receptor 2 (PAR2) agonist (pEC50 = 6.7) that displays no activity at other PAR subtypes or at over 30 other receptors involved in nociception and inflammation. Stimulates cell prolifer... 50mg 3369
TOCRIS BIOSCIENCE		 More Info
AC220 AC220 is a uniquely potent and selective FLT3 inhibitor with IC50 of 0.56 +- 0.3 nM and >10 mM for MC4-11 and A375, respectively. Purity is greater than 99%. 10 mg orb60490
BIORBYT LTD.		 More Info
9-AC n/a 100 mg 0963/100
R&D SYSTEMS, INC.		 More Info
AC 187 Calcitonin and Related Receptor Antagonist 500 µg 3419/500U
R&D SYSTEMS, INC.		 More Info
AC 261066 Retinoic Acid Receptor Agonist 10 mg 4046/10
R&D SYSTEMS, INC.		 More Info
AC 261066 Retinoic Acid Receptor Agonist 50 mg 4046/50
R&D SYSTEMS, INC.		 More Info
AC 264613 Protease-Activated Receptor Agonist 10 mg 3370/10
R&D SYSTEMS, INC.		 More Info
AC 264613 Protease-Activated Receptor Agonist 50 mg 3370/50
R&D SYSTEMS, INC.		 More Info
AC 45594 Nuclear Receptor Antagonist 10 mg 3043/10
R&D SYSTEMS, INC.		 More Info
AC 45594 Nuclear Receptor Antagonist 50 mg 3043/50
R&D SYSTEMS, INC.		 More Info
AC 55541 Protease-Activated Receptor Agonist 10 mg 3369/10
R&D SYSTEMS, INC.		 More Info
AC 55541 Protease-Activated Receptor Agonist 50 mg 3369/50
R&D SYSTEMS, INC.		 More Info
AC 55649 Retinoic Acid Receptor Agonist 10 mg 2436/10
R&D SYSTEMS, INC.		 More Info
AC 55649 Retinoic Acid Receptor Agonist 50 mg 2436/50
R&D SYSTEMS, INC.		 More Info
Ac2-12 Cell Adhesion Inhibitor 1 mg 1846/1
R&D SYSTEMS, INC.		 More Info
Ac2-26 Cell Adhesion Inhibitor 500 µg 1845/500U
R&D SYSTEMS, INC.		 More Info
Ac9-25 Formyl Peptide Receptor Ligand 1 mg 3231/1
R&D SYSTEMS, INC.		 More Info
ACA Calbiochem® brand product. 25mg 104550
EMD MILLIPORE		 More Info
ACAD8 Recombinant Human Acyl-Coenzyme A Dehydrogenase 8 2µg, 10µg, 1mg ENZ- 294
PROSPEC-TANY TECHNOGENE LTD.		 More Info
ACADS Recombinant Human Acyl-Coenzyme A Dehydrogenase, C-2 to C-3 2µg, 10µg, 1mg ENZ- 467
PROSPEC-TANY TECHNOGENE LTD.		 More Info
Acadesine Acadesine is an AMP-activated protein kinase activator which is used for the treatment of acute lymphoblastic leukemia and may have applications in treating other disorders such as diabetes. Purity is greater than 99%. 25 mg orb60688
BIORBYT LTD.		 More Info
ACADM Recombinant Human Acyl-Coenzyme A Dehydrogenase, C-4 to C-12 2µg, 10µg, 1mg ENZ- 529
PROSPEC-TANY TECHNOGENE LTD.		 More Info
Acarbose Minimum Purity: > 98%. Inhibitor of intestinal alpha-glucosidase (IC50 = 11 nM). Antidiabetic; inhibits the hydrolysis of complex carbohydrates. 10mg 2673
TOCRIS BIOSCIENCE		 More Info
Page 4 of 5,777
Records 151 - 200 of 288,813
[1]  «  1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11  »  [5777]
Results per Page: 25 | 50 | 75 | 100
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