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Non-antibody Products (Kits, Proteins, Microbial Antigens, Tissues, Services, etc.) - Page 3 of 5,777
Page 3 of 5,777
Records 101 - 150 of 288,813
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A23187 Purity: >98%. Effective Concentration: 1-10 μM. A23187, Calcimycin, Ca2+ Ionophore A23187, A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic from Streptomyces chartreusen... 10 x 1 mg A-600
ALOMONE LABS
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A23187 Purity: >98%. Effective Concentration: 1-10 μM. A23187, Calcimycin, Ca2+ Ionophore A23187, A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic from Streptomyces chartreusen... 5 x 5 mg A-600
ALOMONE LABS
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A23187 Ca2+ ionophore 10mg Asc-287-10mg
ASCENT SCIENTIFIC LTD.
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A23187 Ca2+ ionophore 50mg Asc-287-50mg
ASCENT SCIENTIFIC LTD.
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A77 1726 Calbiochem® brand product. 5mg 100128
EMD MILLIPORE
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A-71623 Minimum Purity: > 98%. Potent CCK1 agonist (IC50 = 3.7 nM) with 1200-fold selectivity over the CCK2 receptor. Suppresses food intake following central or peripheral administration. 1mg 2411
TOCRIS BIOSCIENCE
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A-769662 A-769662 Purity is greater than 99%. 10 mg orb60992
BIORBYT LTD.
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A-966492 A-966492 is a highly potent and efficacious poly(ADP-ribose) polymerase (PARP) inhibitor with a Ki and EC50 of 1 nM. Purity is greater than 99%. 10 mg orb60826
BIORBYT LTD.
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A23187 A calcium ionophore. Causes rapid influx of calcium in various cells. 10 mg 1501-10
BIOVISION, INC.
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A-769662 Cell-permeable. A potent AMPK activator. Directly stimulates partially purified rat liver AMPK (EC?? = 0.8 µM) and inhibits fatty acid synthesis in primary rat hepatocytes (IC5?? = 3.2 µM). 5 mg 1719-5
BIOVISION, INC.
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A77 1726 Physiologically active metabolite of the immunosuppressive drug leflunomide (Cat. No.1972-10, 50). Inhibits the activity of dihydrorotate dehydrogenase and of protein tyrosine kinases. Blocks TNF-mediated NF-kappaB activation in a dose- and time-d... 5 mg 1973-5
BIOVISION, INC.
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A77 1726 Physiologically active metabolite of the immunosuppressive drug leflunomide (Cat. No.1972-10, 50). Inhibits the activity of dihydrorotate dehydrogenase and of protein tyrosine kinases. Blocks TNF-mediated NF-kappaB activation in a dose- and time-d... 25 mg 1973-25
BIOVISION, INC.
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A-71623 CCK1 Receptor Agonist 1 mg 2411/1
R&D SYSTEMS, INC.
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AA2 n/a n/a n/a
NIH AIDS RESEARCH & REFERENCE REAGENT PROGRAM
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AA 2414 Minimum Purity: > 98%. Thromboxane A2 (TP) receptor antagonist. Antiasthmatic agent; inhibits platelet aggregation and bronchoconstriction induced by a TXA2 mimetic in guinea pigs. 50mg 3025
TOCRIS BIOSCIENCE
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AA 2414 Minimum Purity: > 98%. Thromboxane A2 (TP) receptor antagonist. Antiasthmatic agent; inhibits platelet aggregation and bronchoconstriction induced by a TXA2 mimetic in guinea pigs. 10mg 3025
TOCRIS BIOSCIENCE
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AA 29504 Minimum Purity: > 98%. Positive allosteric modulator of GABAA receptors. Modulates both alpha4beta3delta-containi ng extrasynaptic receptors and alpha1beta3gamma2S-contai ning receptors in Xenopus oocytes, displaying a stronger modulatory effect at ... 10mg 3972
TOCRIS BIOSCIENCE
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AA 29504 Minimum Purity: > 98%. Positive allosteric modulator of GABAA receptors. Modulates both alpha4beta3delta-containi ng extrasynaptic receptors and alpha1beta3gamma2S-contai ning receptors in Xenopus oocytes, displaying a stronger modulatory effect at ... 50mg 3972
TOCRIS BIOSCIENCE
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AA 2414 Prostanoid Receptor Antagonist 10 mg 3025/10
R&D SYSTEMS, INC.
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AA 2414 Prostanoid Receptor Antagonist 50 mg 3025/50
R&D SYSTEMS, INC.
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AA 29504 GABA-A Receptor Modulator 10 mg 3972/10
R&D SYSTEMS, INC.
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AA 29504 GABA-A Receptor Modulator 50 mg 3972/50
R&D SYSTEMS, INC.
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AACOCF3 Phospholipase-A2 inhibitor 5mg Asc-350-5mg
ASCENT SCIENTIFIC LTD.
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AACOCF3 Phospholipase-A2 inhibitor 25mg Asc-350-25mg
ASCENT SCIENTIFIC LTD.
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AACOCF3 Calbiochem® brand product. 10mg 100109
EMD MILLIPORE
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AACOCF3 Minimum Purity: > 98%. Inhibitor of cytosolic (85 kDa) phospholipase A2. Also inhibits fatty acid amide hydrolase (FAAH, anandamide amidase) in vitro. 25mg 1462
TOCRIS BIOSCIENCE
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AACOCF3 Minimum Purity: > 98%. Inhibitor of cytosolic (85 kDa) phospholipase A2. Also inhibits fatty acid amide hydrolase (FAAH, anandamide amidase) in vitro. 5mg 1462
TOCRIS BIOSCIENCE
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AACOCF3 Phospholipase Inhibitor 25 mg 1462/25
R&D SYSTEMS, INC.
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AACOCF3 Phospholipase Inhibitor 5 mg 1462/5
R&D SYSTEMS, INC.
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17-AAG Purity: >99%. Effective Concentration: 50-100 nM. 17-AAG, An Anticancer Antibiotic. 17-AAG is a less toxic and more stable derivative of the antibiotic Geldanamycin. It binds to Hsp90 and regulates its function. Hsp90 regulates the physiology of c... 0.1 mg A-580
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17-AAG Purity: >99%. Effective Concentration: 50-100 nM. 17-AAG, An Anticancer Antibiotic. 17-AAG is a less toxic and more stable derivative of the antibiotic Geldanamycin. It binds to Hsp90 and regulates its function. Hsp90 regulates the physiology of c... 5 x 0.1 mg A-580
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17-AAG Calbiochem® brand product. 500ug 100068
EMD MILLIPORE
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17-AAG Glendanamycin (GA), a benzoquinone ansamycin antibiotic, interferes with the action of Hsp90 leading to degradation of Hsp90 client proteins. GA itself however has undesirable properties such as poor aqueous solubility and liver toxicity; therefor... 1.0mg NB110-81558
NOVUS BIOLOGICALS, LLC
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17-AAG Minimum Purity: > 98%. Inhibitor of heat shock protein 90 (Hsp90) chaperone activity, and an analog of geldanamycin (Cat. No. 1368). Subsequently inhibits the activity of oncogenic proteins such as p185erbB-2 (IC50 = 31 nM), N-ras, Ki-ras and c-Ak... 1mg 1515
TOCRIS BIOSCIENCE
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17-AAG 17-AAG Purity is greater than 99%. 250 mg orb60994
BIORBYT LTD.
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17-AAG Antimicrobial. CAS No.: 75747-14-7 n/a n/a
TOKU-E
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17-AAG A semi-synthetic derivative of Geldanamycin (Cat. No. 1564-1,5) that displays greater stability and lower in vivo toxicity compared to Geldanamycin. Binds to Heat shock protein 90 (Hsp90) (EC?? = 7.2 µM) in a manner similar to geldanamycin. ... 1 mg 1774-1
BIOVISION, INC.
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17-AAG A semi-synthetic derivative of Geldanamycin (Cat. No. 1564-1,5) that displays greater stability and lower in vivo toxicity compared to Geldanamycin. Binds to Heat shock protein 90 (Hsp90) (EC?? = 7.2 µM) in a manner similar to geldanamycin. ... 5 mg 1774-5
BIOVISION, INC.
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17-AAG HSP90 Inhibitor 1 mg 1515/1
R&D SYSTEMS, INC.
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AAPH Calbiochem® brand product. 1gm 100110
EMD MILLIPORE
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ABS 205 Minimum Purity: > 98%. Orally active valproic acid (Cat No. 2815) derivative that exhibits teratogenic and neuroprotective activity. Upregulates neural cell adhesion molecule (NCAM) expression, activates PPARdelta (IC50 = 0.6 mM) and increases Hox... 50mg 2721
TOCRIS BIOSCIENCE
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ABS 205 Minimum Purity: > 98%. Orally active valproic acid (Cat No. 2815) derivative that exhibits teratogenic and neuroprotective activity. Upregulates neural cell adhesion molecule (NCAM) expression, activates PPARdelta (IC50 = 0.6 mM) and increases Hox... 10mg 2721
TOCRIS BIOSCIENCE
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ABS 205 Cell Adhesion Inhibitor 10 mg 2721/10
R&D SYSTEMS, INC.
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ABS 205 Cell Adhesion Inhibitor 50 mg 2721/50
R&D SYSTEMS, INC.
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ABCB5 Purity: Highly Purified. C-QTQHRNTSKKAQ, from the internal region of the protein sequence according to NP_848654.3.Control peptide corresponding to polyclonal antibody, Catalog#A0004-01C, goat x human.Applications: Suitable for use in ELISA. Other... 100ug A0004-01C-P
UNITED STATES BIOLOGICAL
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Abiraterone Abiraterone is a CYP17 inhibitor (IC50 at 4 nM). Purity is greater than 99%. 10 mg orb60159
BIORBYT LTD.
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Abitrexate Abitrexate(Methotrexate) is an antimetabolite and antifolate agent with antineoplastic and immunosuppressant activities. Purity is greater than 99%. 10 mg orb60235
BIORBYT LTD.
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Abltide Peptide sequence (EAIYAAPFAKKK) is based on the C-terminus of Abl. 1 mg A02-58
SIGNALCHEM
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ABTS 2 g; 2,2'-Azino-di-[3-ethylben zthiazoline sulfonate (6)] diammonium salt, crystals. Formula: C18H16N4O6S4-(NH4)2Molecu lar weight: ABTS: Mr = 514.6, ABTS-(NH4)2: Mr = 548.7Solubility: soluble in water (c = 50 mg/ml)Note: The green color is due to f... n/a 10102946001 ROCHE APPLIED SCIENCE More Info
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... 50mg 4138
TOCRIS BIOSCIENCE
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Records 101 - 150 of 288,813
Results per Page: 25 | 50 | 75 | 100
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