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Non-antibody Products (Kits, Proteins, Microbial Antigens, Tissues, Services, etc.) - Page 3 of 6,058
Page 3 of 6,058
Records 101 - 150 of 302,891
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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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A23187 Purity: >98%. A23187 (Calcimycin). Widely Used Ca2+ Ionophore. A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic fromStreptomyces chartreusensis. It is used to increase intrac... 1 mg A-600
ALOMONE LABS
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A23187 Purity: >98%. A23187 (Calcimycin). Widely Used Ca2+ Ionophore. A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic fromStreptomyces chartreusensis. It is used to increase intrac... 10 x 1 mg A-600
ALOMONE LABS
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A23187 Purity: >98%. A23187 (Calcimycin). Widely Used Ca2+ Ionophore. A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic fromStreptomyces chartreusensis. It is used to increase intrac... 5 mg A-600
ALOMONE LABS
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A23187 Purity: >98%. A23187 (Calcimycin). Widely Used Ca2+ Ionophore. A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic fromStreptomyces chartreusensis. It is used to increase intrac... 5 x 5 mg A-600
ALOMONE LABS
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A23187 Purity: >98%. A23187 (Calcimycin). Widely Used Ca2+ Ionophore. A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic fromStreptomyces chartreusensis. It is used to increase intrac... 10 mg A-600
ALOMONE LABS
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A23187 Purity: >98%. 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 chartreusensis. It is used to increase intracellul... 10 x 1 mg A-600
ALOMONE LABS
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A23187 Purity: >98%. 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 chartreusensis. It is used to increase intracellul... 1 mg A-600
ALOMONE LABS
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A23187 Purity: >98%. 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 chartreusensis. It is used to increase intracellul... 5 mg A-600
ALOMONE LABS
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A23187 Purity: >98%. 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 chartreusensis. It is used to increase intracellul... 5 x 5 mg A-600
ALOMONE LABS
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A23187 Purity: >98%. 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 chartreusensis. It is used to increase intracellul... 10 mg A-600
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A-803467 Purity: >99%. A-803467. A Potent and Selective Inhibitor of the TTX-Resistant Na\v\1.8 Channel.The TTX-resistant, Na\v\1.8 channel is expressed almost exclusively in the PNS and has been shown to mediate most of the well documented TTX-resistant c... 5 mg A-105
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A-803467 Purity: >99%. A-803467. A Potent and Selective Inhibitor of the TTX-Resistant Na\v\1.8 Channel.The TTX-resistant, Na\v\1.8 channel is expressed almost exclusively in the PNS and has been shown to mediate most of the well documented TTX-resistant c... 10 mg A-105
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A-803467 Purity: >99%. A-803467. A Potent and Selective Inhibitor of the TTX-Resistant Na\v\1.8 Channel.The TTX-resistant, Na\v\1.8 channel is expressed almost exclusively in the PNS and has been shown to mediate most of the well documented TTX-resistant c... 25 mg A-105
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A-803467 Purity: >99%. A-803467. A Potent and Selective Inhibitor of the TTX-Resistant Na\v\1.8 Channel.The TTX-resistant, Na\v\1.8 channel is expressed almost exclusively in the PNS and has been shown to mediate most of the well documented TTX-resistant c... 50 mg A-105
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A-803467 Purity: >99%. A-803467. A Potent and Selective Inhibitor of the TTX-Resistant Na\v\1.8 Channel.The TTX-resistant, Na\v\1.8 channel is expressed almost exclusively in the PNS and has been shown to mediate most of the well documented TTX-resistant c... 100 mg A-105
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A-71623 Potent CCK1 agonist (IC50 = 3.7 nM) with 1200-fold selectivity over the CCK2 receptor. Suppresses food intake following central or peripheral administration. Minimum Purity: > 98% 1mg 2411
TOCRIS BIOSCIENCE
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A-769662 MW: 360.39 Da. CAS number: [8444499-71-4]. Formula: C20H12N2O3S. Solubility: Soluble in DMSO at 33 mg/mL; soluble in ethanol at 5 mg/mL with slight warming; very poorly soluble in water; maximum solubility in plain water is estimated to be about 5... 50 mg orb61202
BIORBYT LTD.
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A77 1726 Molecular Weight: 270.2. White solid. Packaged under inert gas. 5 mg 100128-5MG
EMD MILLIPORE
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AA2 n/a n/a n/a
NIH AIDS RESEARCH & REFERENCE REAGENT PROGRAM
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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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Aa1 Purity: >98%. Aa1. A Novel Blocker of Shaker-B and IA K+ Channels. Native Aa1 was originally isolated from Androctonus australis scorpion venom. Aa1 is a recombinant peptide expressed in and extracted from E. coli and purified to homogeneity. Nati... 5 µg RTA-400
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Aa1 Purity: >98%. Aa1. A Novel Blocker of Shaker-B and IA K+ Channels. Native Aa1 was originally isolated from Androctonus australis scorpion venom. Aa1 is a recombinant peptide expressed in and extracted from E. coli and purified to homogeneity. Nati... 5 x 5 µg RTA-400
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Aa1 Purity: >98%. Aa1. A Novel Blocker of Shaker-B and IA K+ Channels. Native Aa1 was originally isolated from Androctonus australis scorpion venom. Aa1 is a recombinant peptide expressed in and extracted from E. coli and purified to homogeneity. Nati... 10 µg RTA-400
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Aa1 Purity: >98%. Aa1. A Novel Blocker of Shaker-B and IA K+ Channels. Native Aa1 was originally isolated from Androctonus australis scorpion venom. Aa1 is a recombinant peptide expressed in and extracted from E. coli and purified to homogeneity. Nati... 5 x 10 µg RTA-400
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Aa1 Purity: >98%. Aa1. A Novel Blocker of Shaker-B and IA K+ Channels. Native Aa1 was originally isolated from Androctonus australis scorpion venom. Aa1 is a recombinant peptide expressed in and extracted from E. coli and purified to homogeneity. Nati... 0.1 mg RTA-400
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AA 2414 Thromboxane A2 (TP) receptor antagonist. Antiasthmatic agent; inhibits platelet aggregation and bronchoconstriction induced by a TXA2 mimetic in guinea pigs. Minimum Purity: > 98% 10mg 3025
TOCRIS BIOSCIENCE
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AA 2414 Thromboxane A2 (TP) receptor antagonist. Antiasthmatic agent; inhibits platelet aggregation and bronchoconstriction induced by a TXA2 mimetic in guinea pigs. Minimum Purity: > 98% 50mg 3025
TOCRIS BIOSCIENCE
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AA 29504 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 the former. Reduces mot... 10mg 3972
TOCRIS BIOSCIENCE
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AA 29504 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 the former. Reduces mot... 50mg 3972
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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AACOCF3 Inhibitor of cytosolic (85 kDa) phospholipase A2. Also inhibits fatty acid amide hydrolase (FAAH, anandamide amidase) in vitro. Minimum Purity: > 98% 25mg 1462
TOCRIS BIOSCIENCE
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AACOCF3 Inhibitor of cytosolic (85 kDa) phospholipase A2. Also inhibits fatty acid amide hydrolase (FAAH, anandamide amidase) in vitro. Minimum Purity: > 98% 5mg 1462
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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17-AAG Purity: >99%. 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 cells exposed to environmental stress... 0.1 mg A-580
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17-AAG Purity: >99%. 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 cells exposed to environmental stress... 5 x 0.1 mg A-580
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17-AAG 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-Akt. Antitumor in vivo. M... 1mg 1515
TOCRIS BIOSCIENCE
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Results per Page: 25 | 50 | 75 | 100
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