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Non-antibody Products (Kits, Proteins, Microbial Antigens, Tissues, Services, etc.) - Page 4 of 5,777
| 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
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| 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
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| 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
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| 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
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| 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
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| 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
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| 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
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| 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
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