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Non-antibody Products (Kits, Proteins, Microbial Antigens, Tissues, Services, etc.) - Page 9 of 5,777
Page 9 of 5,777
Records 401 - 450 of 288,813
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Name Description Size Catalog # Supplier  
AG 490 Minimum Purity: > 99%. Selective inhibitor of EGF receptor tyrosine kinase (IC50 values are 2 and 13.5 µM for EGFR and ErbB2 respectively). Inhibitor of JAK2, JAK3/STAT, JAK3/AP-1 and JAK3/MAPK pathways and potently inhibits cytokine-indepen... 10mg 414
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AG 490 Minimum Purity: > 99%. Selective inhibitor of EGF receptor tyrosine kinase (IC50 values are 2 and 13.5 µM for EGFR and ErbB2 respectively). Inhibitor of JAK2, JAK3/STAT, JAK3/AP-1 and JAK3/MAPK pathways and potently inhibits cytokine-indepen... 50mg 414
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AG 555 Minimum Purity: > 99%. Potent epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 0.7 µM) that displays 50-fold and >140-fold selectivity over ErbB2 and insulin receptor kinase respectively. Induce G1 growth arrest selectively i... 10mg 618
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AG 555 Minimum Purity: > 99%. Potent epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 0.7 µM) that displays 50-fold and >140-fold selectivity over ErbB2 and insulin receptor kinase respectively. Induce G1 growth arrest selectively i... 50mg 618
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AG 556 Minimum Purity: > 99%. Epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 1.1 µM). Selective over ErbB2 (IC50 > 500 µM). 10mg 616
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AG 556 Minimum Purity: > 99%. Epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 1.1 µM). Selective over ErbB2 (IC50 > 500 µM). 50mg 616
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AG 825 Minimum Purity: > 98%. Selective ErbB2 inhibitor (IC50 values are 0.15 and 19 mM at ErbB2 and ErbB1 respectively). Preferentially triggers p38 MAP kinase-dependent apoptosis in androgen-independent prostate cancer cells. 10mg 1555
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AG 825 Minimum Purity: > 98%. Selective ErbB2 inhibitor (IC50 values are 0.15 and 19 mM at ErbB2 and ErbB1 respectively). Preferentially triggers p38 MAP kinase-dependent apoptosis in androgen-independent prostate cancer cells. 50mg 1555
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AG 879 Minimum Purity: > 99%. Inhibitor of the tyrosine kinase activity of nerve growth factor (NGF) TrkA. Decreases cellular proliferation in human muscular sarcoma cell lines. Also inhibits ErbB2 and VEGFR-2 (IC50 values are approximately 1 µM fo... 10mg 2617
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AG 99 Minimum Purity: > 99%. Epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 10 µM) that is selective over insulin receptor kinase. Blocks tyrosine phosphorylation of p145met and promotes cell death of normal and cancer cells via ... 10mg 497
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AG 99 Minimum Purity: > 99%. Epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 10 µM) that is selective over insulin receptor kinase. Blocks tyrosine phosphorylation of p145met and promotes cell death of normal and cancer cells via ... 50mg 497
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AG 494 Minimum Purity: > 98%. Potent inhibitor of epidermal growth factor receptor (EGFR) kinase (IC50 = 0.7 µM). Selective over ErbB2, PDGFR and insulin receptor kinase (IC50 values are 42, 6 and > 100 µM respectively). 10mg 619
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AG 494 Minimum Purity: > 98%. Potent inhibitor of epidermal growth factor receptor (EGFR) kinase (IC50 = 0.7 µM). Selective over ErbB2, PDGFR and insulin receptor kinase (IC50 values are 42, 6 and > 100 µM respectively). 50mg 619
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AG 045572 Minimum Purity: > 98%. Selective gonadotropin-releasing hormone (GnRH) receptor antagonist (Ki values are 2.2, 3.8 and 6.0 nM for mouse, rat and human receptors respectively). Suppresses testosterone and luteinising hormone (LH) levels in vivo. 1mg 2730
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AG 045572 Minimum Purity: > 98%. Selective gonadotropin-releasing hormone (GnRH) receptor antagonist (Ki values are 2.2, 3.8 and 6.0 nM for mouse, rat and human receptors respectively). Suppresses testosterone and luteinising hormone (LH) levels in vivo. 10mg 2730
TOCRIS BIOSCIENCE
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AG-014699 AG-014699 is a PARP inhibitor (Ki, 1.4 nmol/L). Purity is greater than 99%. 5 mg orb60138
BIORBYT LTD.
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AG14361 AG14361 is a potent poly(ADP-ribose) polymerase (PARP-1) inhibitor with a GI50 of 10.9 ?M. Purity is greater than 99%. 10 mg orb60811
BIORBYT LTD.
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AG-490 AG 490 is a potent epidermal growth factor receptor kinase autophosphorylation inhibitor with an IC50 of 100 nM and 56.8 ?M for EGFR and JAK, respectively. Purity is greater than 99%. 25 mg orb60171
BIORBYT LTD.
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AG 1478 Cell-permeable. A potent EGFR Tyrosine Kinase (TK) inhibitor with an IC50 of 3 nM. Only weakly inhibits PDGFR and HER2-NEU kinases (IC50 >100 µM). 5 mg 1800-5
BIOVISION, INC.
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AG 1478 Cell-permeable. A potent EGFR Tyrosine Kinase (TK) inhibitor with an IC50 of 3 nM. Only weakly inhibits PDGFR and HER2-NEU kinases (IC50 >100 µM). 25 mg 1800-25
BIOVISION, INC.
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AG 045572 GnRH Receptor Antagonist 1 mg 2730/1
R&D SYSTEMS, INC.
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AG 045572 GnRH Receptor Antagonist 10 mg 2730/10
R&D SYSTEMS, INC.
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AG 18 EGF Receptor Inhibitor 10 mg 0493/10
R&D SYSTEMS, INC.
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AG 18 EGF Receptor Inhibitor 50 mg 0493/50
R&D SYSTEMS, INC.
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AG 213 EGF Receptor Inhibitor 10 mg 0503/10
R&D SYSTEMS, INC.
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AG 213 EGF Receptor Inhibitor 50 mg 0503/50
R&D SYSTEMS, INC.
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AG 490 EGF Receptor Inhibitor 10 mg 0414/10
R&D SYSTEMS, INC.
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AG 490 EGF Receptor Inhibitor 50 mg 0414/50
R&D SYSTEMS, INC.
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AG 494 EGF Receptor Inhibitor 10 mg 0619/10
R&D SYSTEMS, INC.
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AG 494 EGF Receptor Inhibitor 50 mg 0619/50
R&D SYSTEMS, INC.
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AG 555 EGF Receptor Inhibitor 10 mg 0618/10
R&D SYSTEMS, INC.
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AG 555 EGF Receptor Inhibitor 50 mg 0618/50
R&D SYSTEMS, INC.
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AG 556 EGF Receptor Inhibitor 10 mg 0616/10
R&D SYSTEMS, INC.
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AG 556 EGF Receptor Inhibitor 50 mg 0616/50
R&D SYSTEMS, INC.
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AG 825 EGF Receptor Inhibitor 10 mg 1555/10
R&D SYSTEMS, INC.
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AG 825 EGF Receptor Inhibitor 50 mg 1555/50
R&D SYSTEMS, INC.
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AG 879 Trk Receptor Inhibitor 10 mg 2617/10
R&D SYSTEMS, INC.
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AG 99 EGF Receptor Inhibitor 10 mg 0497/10
R&D SYSTEMS, INC.
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AG 99 EGF Receptor Inhibitor 50 mg 0497/50
R&D SYSTEMS, INC.
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AGAR n/a n/a n/a AMERICAN BIOANALYTICAL More Info
Agar Calbiochem® brand product. 1kg 12177
EMD MILLIPORE
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Agarase Agarase cleaves agarose to neoagaro-oligosaccharides , and is used for quantitative, gentle recovery of DNA from low melting point agarose. 500 units 9201-500
BIOVISION, INC.
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AGK 2 Minimum Purity: > 98%. Selective inhibitor of SIRT2 (IC50 = 3.5 µM). Displays no activity at SIRT1 and SIRT3 at concentrations up to 40 µM. Reduces alpha-synuclein-mediated toxicity in in vitro and in vivo models of Parkinson's disease. 10mg 3233
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AGK 2 Minimum Purity: > 98%. Selective inhibitor of SIRT2 (IC50 = 3.5 µM). Displays no activity at SIRT1 and SIRT3 at concentrations up to 40 µM. Reduces alpha-synuclein-mediated toxicity in in vitro and in vivo models of Parkinson's disease. 50mg 3233
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AGK 2 Sir2-like Family Deacetylase Inhibitor 10 mg 3233/10
R&D SYSTEMS, INC.
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AGK 2 Sir2-like Family Deacetylase Inhibitor 50 mg 3233/50
R&D SYSTEMS, INC.
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Agomelatine Agomelatine is classified as a norepinephrine-dopamine disinhibitor (NDDI) due to its antagonism of the 5-HT2C receptor. Purity is greater than 99%. 10 mg orb60262
BIORBYT LTD.
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AGR2 Recombinant Human Anterior Gradient Protein 2 Homolog 10µg, 50µg, 1mg PRO- 580
PROSPEC-TANY TECHNOGENE LTD.
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AGRP Recombinant Human Agouti-Related Protein 2µg, 10µg, 1mg HOR- 283
PROSPEC-TANY TECHNOGENE LTD.
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AH 6809 Minimum Purity: > 99%. Antagonist at prostaglandin EP1 (pA2 = 6.8) and EP2 (Ki = 350 nM) receptors. Also weakly inhibits DP receptors (pA2 = 4.45). 50mg 671
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Page 9 of 5,777
Records 401 - 450 of 288,813
Results per Page: 25 | 50 | 75 | 100
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