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Non-antibody Products (Kits, Proteins, Microbial Antigens, Tissues, Services, etc.) - Page 1 of 5,777
Page 1 of 5,777
Records 1 - 50 of 288,813
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Name Description Size Catalog # Supplier  
AS 101 Minimum Purity: > 98%. Immunomodulator; inhibits IL-10 synthesis and potentiates IL-1alpha, IL-2 and TNF-alpha release. 50mg 2446
TOCRIS BIOSCIENCE		 More Info
AS 101 Minimum Purity: > 98%. Immunomodulator; inhibits IL-10 synthesis and potentiates IL-1alpha, IL-2 and TNF-alpha release. 10mg 2446
TOCRIS BIOSCIENCE		 More Info
AT 101 Minimum Purity: > 98%. R-(-)-enantiomer of gossypol (Cat. No. 1964). Mimics the BH3 domains of Bcl-2, Bcl-XL and Mcl-1. Disrupts heterodimerization of Bcl-2 with proapoptotic family members. Induces apoptosis in vitro through activation of caspase... 50mg 3367
TOCRIS BIOSCIENCE		 More Info
AT 101 Minimum Purity: > 98%. R-(-)-enantiomer of gossypol (Cat. No. 1964). Mimics the BH3 domains of Bcl-2, Bcl-XL and Mcl-1. Disrupts heterodimerization of Bcl-2 with proapoptotic family members. Induces apoptosis in vitro through activation of caspase... 10mg 3367
TOCRIS BIOSCIENCE		 More Info
AS 101 n/a 10 mg 2446/10
R&D SYSTEMS, INC.		 More Info
AS 101 n/a 50 mg 2446/50
R&D SYSTEMS, INC.		 More Info
AT 101 n/a 10 mg 3367/10
R&D SYSTEMS, INC.		 More Info
AT 101 n/a 50 mg 3367/50
R&D SYSTEMS, INC.		 More Info
A 1120 Minimum Purity: > 99%. High affinity retinol-binding protein 4 (RBP4) ligand (Ki = 8.3 nM); non-retinoid. Selective against a range of different cellular targets. As efficacious as fenretinide (Cat. No. 1396) in the reduction of serum RBP4 and ret... 50mg 3793
TOCRIS BIOSCIENCE		 More Info
A 1120 Minimum Purity: > 99%. High affinity retinol-binding protein 4 (RBP4) ligand (Ki = 8.3 nM); non-retinoid. Selective against a range of different cellular targets. As efficacious as fenretinide (Cat. No. 1396) in the reduction of serum RBP4 and ret... 10mg 3793
TOCRIS BIOSCIENCE		 More Info
A 1120 n/a 10 mg 3793/10
R&D SYSTEMS, INC.		 More Info
A 1120 n/a 50 mg 3793/50
R&D SYSTEMS, INC.		 More Info
AS 1269574 Minimum Purity: > 98%. GPR119 receptor agonist (EC50 = 2.5 µM in HEK293 cells expressing human GPR119). Enhances insulin secretion stimulated by glucose in vivo. Orally available. 50mg 4177
TOCRIS BIOSCIENCE		 More Info
AS 1269574 Minimum Purity: > 98%. GPR119 receptor agonist (EC50 = 2.5 µM in HEK293 cells expressing human GPR119). Enhances insulin secretion stimulated by glucose in vivo. Orally available. 10mg 4177
TOCRIS BIOSCIENCE		 More Info
AS 1269574 GPR119 Receptor Agonist 10 mg 4177/10
R&D SYSTEMS, INC.		 More Info
AS 1269574 GPR119 Receptor Agonist 50 mg 4177/50
R&D SYSTEMS, INC.		 More Info
AS 19 Minimum Purity: > 98%. Potent 5-HT7 receptor agonist (IC50 = 0.83 nM). Enhances memory consolidation and reverses scopolamine- or dizocilpine-induced amnesia in vivo. 10mg 1968
TOCRIS BIOSCIENCE		 More Info
AS 19 Minimum Purity: > 98%. Potent 5-HT7 receptor agonist (IC50 = 0.83 nM). Enhances memory consolidation and reverses scopolamine- or dizocilpine-induced amnesia in vivo. 50mg 1968
TOCRIS BIOSCIENCE		 More Info
AS 19 5-HT7 Receptor Agonist 10 mg 1968/10
R&D SYSTEMS, INC.		 More Info
AS 19 5-HT7 Receptor Agonist 50 mg 1968/50
R&D SYSTEMS, INC.		 More Info
AS 1949490 Minimum Purity: > 99%. Selective SHIP2 (SH2 domain-containing inositol 5'-phosphatase 2) inhibitor (IC50 values are 0.34 µM and 0.62 µM for mouse and human respectively); displays approximately 30-fold affinity for SHIP2 over SHIP1. In... 10mg 3718
TOCRIS BIOSCIENCE		 More Info
AS 1949490 Minimum Purity: > 99%. Selective SHIP2 (SH2 domain-containing inositol 5'-phosphatase 2) inhibitor (IC50 values are 0.34 µM and 0.62 µM for mouse and human respectively); displays approximately 30-fold affinity for SHIP2 over SHIP1. In... 50mg 3718
TOCRIS BIOSCIENCE		 More Info
AS 1949490 Inositol Phosphatase Inhibitor 10 mg 3718/10
R&D SYSTEMS, INC.		 More Info
AS 1949490 Inositol Phosphatase Inhibitor 50 mg 3718/50
R&D SYSTEMS, INC.		 More Info
A 205804 Minimum Purity: > 98%. Selective inhibitor of E-selectin and ICAM-1 expression (IC50 values are 20, 25 and > 1000 nM for TNF-alpha-induced E-selectin, ICAM-1 and VCAM-1 expression respectively). Effective inhibitor of cell-cell adhesion in an in v... 10mg 2524
TOCRIS BIOSCIENCE		 More Info
A 205804 Minimum Purity: > 98%. Selective inhibitor of E-selectin and ICAM-1 expression (IC50 values are 20, 25 and > 1000 nM for TNF-alpha-induced E-selectin, ICAM-1 and VCAM-1 expression respectively). Effective inhibitor of cell-cell adhesion in an in v... 50mg 2524
TOCRIS BIOSCIENCE		 More Info
A 205804 Cell Adhesion Inhibitor 10 mg 2524/10
R&D SYSTEMS, INC.		 More Info
A 205804 Cell Adhesion Inhibitor 50 mg 2524/50
R&D SYSTEMS, INC.		 More Info
S 24795 Minimum Purity: > 98%. Partial agonist of alpha7 nAChR. Improves mnemonic function in aged mice for the treatment of aging-related memory disturbances. Displays more efficient memory-enhancing effects than memantine (Cat.No 0773) in Alzheimer's di... 50mg 3518
TOCRIS BIOSCIENCE		 More Info
S 24795 Minimum Purity: > 98%. Partial agonist of alpha7 nAChR. Improves mnemonic function in aged mice for the treatment of aging-related memory disturbances. Displays more efficient memory-enhancing effects than memantine (Cat.No 0773) in Alzheimer's di... 10mg 3518
TOCRIS BIOSCIENCE		 More Info
S 24795 Nicotinic (a7) Receptor Agonist 10 mg 3518/10
R&D SYSTEMS, INC.		 More Info
S 24795 Nicotinic (a7) Receptor Agonist 50 mg 3518/50
R&D SYSTEMS, INC.		 More Info
AS 252424 Minimum Purity: > 98%. Potent and selective inhibitor of PI 3-kinase gamma (IC50 values are 33 and 935 nM for PI3Kgamma and PI3Kalpha respectively). 10mg 3671
TOCRIS BIOSCIENCE		 More Info
AS 252424 PI 3-Kinase Inhibitor 10 mg 3671/10
R&D SYSTEMS, INC.		 More Info
S 25585 Minimum Purity: > 98%. Potent neuropeptide Y (NPY) Y5 receptor antagonist (IC50 values are 5.4, > 1000, > 10 000 and > 10 000 nM at Y5, Y1, Y2 and Y4 receptors respectively) that displays no affinity for a wide range of other receptors. Does not p... 10mg 3432
TOCRIS BIOSCIENCE		 More Info
S 25585 Minimum Purity: > 98%. Potent neuropeptide Y (NPY) Y5 receptor antagonist (IC50 values are 5.4, > 1000, > 10 000 and > 10 000 nM at Y5, Y1, Y2 and Y4 receptors respectively) that displays no affinity for a wide range of other receptors. Does not p... 50mg 3432
TOCRIS BIOSCIENCE		 More Info
S 25585 NPY Receptor Antagonist 10 mg 3432/10
R&D SYSTEMS, INC.		 More Info
S 25585 NPY Receptor Antagonist 50 mg 3432/50
R&D SYSTEMS, INC.		 More Info
A 286982 Minimum Purity: > 99%. Potent inhibitor of the LFA-1/ICAM-1 interaction (IC50 values are 44 and 35 nM in LFA-1/ICAM-1 binding and LFA-1-mediated cell adhesion assays respectively). 10mg 4228
TOCRIS BIOSCIENCE		 More Info
A 286982 Minimum Purity: > 99%. Potent inhibitor of the LFA-1/ICAM-1 interaction (IC50 values are 44 and 35 nM in LFA-1/ICAM-1 binding and LFA-1-mediated cell adhesion assays respectively). 50mg 4228
TOCRIS BIOSCIENCE		 More Info
A 286982 Integrin Receptor Inhibitor 10 mg 4228/10
R&D SYSTEMS, INC.		 More Info
A 286982 Integrin Receptor Inhibitor 50 mg 4228/50
R&D SYSTEMS, INC.		 More Info
293 n/a n/a n/a
NIH AIDS RESEARCH & REFERENCE REAGENT PROGRAM		 More Info
293 n/a n/a n/a VIRCELL S.L. More Info
S 32826 Minimum Purity: > 98%. Inhibitor of autotaxin (IC50 = 9 nM). Displays similar inhibitory effects at all three autotaxin isoforms (alpha, beta and gamma). Exhibits no affinity for lysophosphatidic acid receptor 1 (LPA1) at concentrations up to 10 &... 10mg 3404
TOCRIS BIOSCIENCE		 More Info
S 32826 Autotaxin Inhibitor 10 mg 3404/10
R&D SYSTEMS, INC.		 More Info
AT 56 Minimum Purity: > 99%. Orally active inhibitor of lipocalin-type prostaglandin D synthase (L-PGDS) (Ki = 75 µM, IC50 = 95 µM). Inhibits the production of PGD2 from PGH2 in vitro, with no effect on PGE2 or PGF2alpha production. 10mg 3531
TOCRIS BIOSCIENCE		 More Info
AT 56 Minimum Purity: > 99%. Orally active inhibitor of lipocalin-type prostaglandin D synthase (L-PGDS) (Ki = 75 µM, IC50 = 95 µM). Inhibits the production of PGD2 from PGH2 in vitro, with no effect on PGE2 or PGF2alpha production. 50mg 3531
TOCRIS BIOSCIENCE		 More Info
AT 56 Synthase/Synthetase Inhibitor 10 mg 3531/10
R&D SYSTEMS, INC.		 More Info
AT 56 Synthase/Synthetase Inhibitor 50 mg 3531/50
R&D SYSTEMS, INC.		 More Info
Page 1 of 5,777
Records 1 - 50 of 288,813
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Results per Page: 25 | 50 | 75 | 100
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