Link To Us Link To Us

Bookmark Us Bookmark Us

Supplier Login Supplier Login

Linscott's Directory of Immunological & Biological Reagents
Search Non-Antibody Products
Search Tips:
Non-antibody Products (Kits, Proteins, Microbial Antigens, Tissues, Services, etc.) - Page 31 of 6,058
Page 31 of 6,058
Records 1,501 - 1,550 of 302,891
[1]  «  26 | 27 | 28 | 29 | 30 | 31 | 32 | 33 | 34 | 35 | 36  »  [6058]
Results per Page: 25 | 50 | 75 | 100
Name Description Size Catalog # Supplier  
Block Ace n/a 20 x 4 g YSRTBUF029
ACCURATE CHEMICAL & SCIENTIFIC CO.		 More Info
AGKISTRODON BLOMHOFFI reptile venom n/a n/a MIAMI SERPENTARIUM LABS More Info
alamarBlue alamarBlue is an indicator dye, that incorporates an oxidation-reduction (REDOX) indicator that both fluoresces and changes colour in response to the chemical reduction of growth medium, resulting from cell growth. The alamarBlue assay is designed... 100 ml MBS238968
MYBIOSOURCE, LLC		 More Info
BMY 14802 General Sigma Receptor Antagonist 10 mg 1440/10
R&D SYSTEMS, INC.		 More Info
BMY 14802 General Sigma Receptor Antagonist 50 mg 1440/50
R&D SYSTEMS, INC.		 More Info
BMY 45778 Prostanoid Receptor Agonist 10 mg 1442/10
R&D SYSTEMS, INC.		 More Info
BMY 45778 Prostanoid Receptor Agonist 50 mg 1442/50
R&D SYSTEMS, INC.		 More Info
BMY 45778 Non-prostanoid prostacyclin mimetic that acts as a partial agonist at IP1 prostacyclin receptors. Potently inhibits platelet aggregation in vitro (IC50 = 27-35 nM). Minimum Purity: > 99% 50mg 1442
TOCRIS BIOSCIENCE		 More Info
BMY 45778 Non-prostanoid prostacyclin mimetic that acts as a partial agonist at IP1 prostacyclin receptors. Potently inhibits platelet aggregation in vitro (IC50 = 27-35 nM). Minimum Purity: > 99% 10mg 1442
TOCRIS BIOSCIENCE		 More Info
BML-190 Cannabinoid R2/CB2 Receptor Ligand 10 mg 1383/10
R&D SYSTEMS, INC.		 More Info
BML-190 Cannabinoid R2/CB2 Receptor Ligand 50 mg 1383/50
R&D SYSTEMS, INC.		 More Info
BML-190 Potent and selective CB2 receptor ligand (Ki values are 435 nM and > 2 µM for CB2 and CB1 respectively). Minimum Purity: > 99% 10mg 1383
TOCRIS BIOSCIENCE		 More Info
BML-190 Potent and selective CB2 receptor ligand (Ki values are 435 nM and > 2 µM for CB2 and CB1 respectively). Minimum Purity: > 99% 50mg 1383
TOCRIS BIOSCIENCE		 More Info
BML-210 Inhibition of histone deacetylase (HDAC) enzymes by compounds such as trichostatin A can have wide ranging effects in cancer, cell differentiation, and other aspects of gene expression regulation. BML-210 is a small molecule inhibitor of HDAC with... 5 mg P013-5MG
ARBOR ASSAYS, LLC		 More Info
BML-210 Inhibition of histone deacetylase (HDAC) enzymes by compounds such as trichostatin A can have wide ranging effects in cancer, cell differentiation, and other aspects of gene expression regulation. BML-210 is a small molecule inhibitor of HDAC with... 25 mg P013-25MG
ARBOR ASSAYS, LLC		 More Info
BML-278 Sirt activator based on a dihydropyridine structural scaffold. EC150 (effective concentration able to increase enzyme activity by 150%) is 1 uM for Sirt1, 25 uM for Sirt2, and 50 uM for Sirt3. The compound is active in whole cells and arrests cell... 5 mg P003-5MG
ARBOR ASSAYS, LLC		 More Info
BML-278 Sirt activator based on a dihydropyridine structural scaffold. EC150 (effective concentration able to increase enzyme activity by 150%) is 1 uM for Sirt1, 25 uM for Sirt2, and 50 uM for Sirt3. The compound is active in whole cells and arrests cell... 25 mg P003-25MG
ARBOR ASSAYS, LLC		 More Info
BMP3 Purity: >95% 50 µg AR20013PU-N
ACRIS ANTIBODIES GmbH		 More Info
BMP3 Purity: >95% 10 µg AR20013PU-S
ACRIS ANTIBODIES GmbH		 More Info
BMP3 Purity: >95% 20 µg AR09436PU-N
ACRIS ANTIBODIES GmbH		 More Info
BMP3 Purity: >95% 5 µg AR09436PU-S
ACRIS ANTIBODIES GmbH		 More Info
BMS 777607 BMS 777607 is a Small-Molecule Met Kinase Inhibitor with an IC50 of < 0.1 ?M. Purity is greater than 99%. 10 mg orb60514
BIORBYT LTD.		 More Info
BMS 794833 BMS-794833 is a potent ATPcompetitive Met/VEGFR-2 kinase inhibitor and it also inhibits Ron (Met family),Axl and Flt-3 with IC50 values <3 nM. Purity is greater than 99%. 10 mg orb60830
BIORBYT LTD.		 More Info
BMS-536924 BMS-536924 Purity is greater than 99%. 10 mg orb60073
BIORBYT LTD.		 More Info
BMS-599626 BMS-599626 is a highly selective pan-HERKinase inhibitor with IC50 of 20 and 30 nM for the inhibition of HER1and HER2, respectively. Purity is greater than 99%. 5 mg orb60108
BIORBYT LTD.		 More Info
BMS-707035 BMS-707035 is an HIV-1 integrase (IN) inhibitor. Purity is greater than 99%. 10 mg orb60354
BIORBYT LTD.		 More Info
BMS-708163 ?-secretase inhibitor (GSI) (IC50 =0.3 nM) Purity is greater than 99%. 10 mg orb60280
BIORBYT LTD.		 More Info
BMS-740808 BMS-740808 is a highly potent, selective, efficacious, and orally bioavailable blood coagulation factor Xa inhibitor with a Ki of 30 pM. Purity is greater than 99%. 10 mg orb60520
BIORBYT LTD.		 More Info
BMS-790052 BMS-790052 is a first-in-class, highly-selective oral HCV NS5A inhibitor. Purity is greater than 99%. 10 mg orb60456
BIORBYT LTD.		 More Info
BMS-599626 An orally bioavailable pan-HER tyrosine kinase inhibitor with potential antineoplastic activity. BMS-599626 inhibits human epidermal growth factor receptors (HER) HER1, HER2 and HER4, thereby inhibiting the proliferation of tumor cells that overex... 1 mg 1614-1
BIOVISION, INC.		 More Info
BMS-599626 An orally bioavailable pan-HER tyrosine kinase inhibitor with potential antineoplastic activity. BMS-599626 inhibits human epidermal growth factor receptors (HER) HER1, HER2 and HER4, thereby inhibiting the proliferation of tumor cells that overex... 5 mg 1614-5
BIOVISION, INC.		 More Info
BMS 191011 Ca2+-Activated Potassium Channel Activator 10 mg 2665/10
R&D SYSTEMS, INC.		 More Info
BMS 191011 Ca2+-Activated Potassium Channel Activator 50 mg 2665/50
R&D SYSTEMS, INC.		 More Info
BMS 193885 NPY Receptor Antagonist 10 mg 3242/10
R&D SYSTEMS, INC.		 More Info
BMS 193885 NPY Receptor Antagonist 50 mg 3242/50
R&D SYSTEMS, INC.		 More Info
BMS 195614 Retinoic Acid Receptor Antagonist 10 mg 3660/10
R&D SYSTEMS, INC.		 More Info
BMS 195614 Retinoic Acid Receptor Antagonist 50 mg 3660/50
R&D SYSTEMS, INC.		 More Info
BMS 299897 Secretase Inhibitor 10 mg 2870/10
R&D SYSTEMS, INC.		 More Info
BMS 453 n/a 10 mg 3409/10
R&D SYSTEMS, INC.		 More Info
BMS 493 Retinoic Acid Receptor Antagonist 10 mg 3509/10
R&D SYSTEMS, INC.		 More Info
BMS 493 Retinoic Acid Receptor Antagonist 50 mg 3509/50
R&D SYSTEMS, INC.		 More Info
BMS 753 Retinoic Acid Receptor Agonist 10 mg 3505/10
R&D SYSTEMS, INC.		 More Info
BMS 753 Retinoic Acid Receptor Agonist 50 mg 3505/50
R&D SYSTEMS, INC.		 More Info
BMS 961 Retinoic Acid Receptor Agonist 10 mg 3410/10
R&D SYSTEMS, INC.		 More Info
BMS 961 Retinoic Acid Receptor Agonist 50 mg 3410/50
R&D SYSTEMS, INC.		 More Info
BMS 191011 Potent Maxi-K channel opener (large-conductance Ca2+-activated potassium channel, KCa1.1, BKCa). Neuroprotectant in two distinct animal models of stroke (MCAO in the SHR rat and a normotensive model of focal stroke). Minimum Purity: > 99% 50mg 2665
TOCRIS BIOSCIENCE		 More Info
BMS 191011 Potent Maxi-K channel opener (large-conductance Ca2+-activated potassium channel, KCa1.1, BKCa). Neuroprotectant in two distinct animal models of stroke (MCAO in the SHR rat and a normotensive model of focal stroke). Minimum Purity: > 99% 10mg 2665
TOCRIS BIOSCIENCE		 More Info
BMS 193885 Potent, competitive neuropeptide (NPY) Y1 antagonist (Ki = 3.3 nM, IC50 = 5.9 nM) that displays > 47, > 100, > 160, > 160 and > 160-fold selectivity over ?1, alpha1, Y2, Y4 and Y5 receptors respectively. Reduces food intake and body weight via cen... 10mg 3242
TOCRIS BIOSCIENCE		 More Info
BMS 193885 Potent, competitive neuropeptide (NPY) Y1 antagonist (Ki = 3.3 nM, IC50 = 5.9 nM) that displays > 47, > 100, > 160, > 160 and > 160-fold selectivity over ?1, alpha1, Y2, Y4 and Y5 receptors respectively. Reduces food intake and body weight via cen... 50mg 3242
TOCRIS BIOSCIENCE		 More Info
BMS 195614 Neutral retinoic acid receptor (RAR) alpha-selective antagonist (Ki = 2.5 nM). Displays no significant effect on nuclear receptor corepressor (NCoR) binding; moderately decreases SMRT binding to RAR. Antagonizes agonist-induced coactivator (CoA) r... 10mg 3660
TOCRIS BIOSCIENCE		 More Info
Page 31 of 6,058
Records 1,501 - 1,550 of 302,891
[1]  «  26 | 27 | 28 | 29 | 30 | 31 | 32 | 33 | 34 | 35 | 36  »  [6058]
Results per Page: 25 | 50 | 75 | 100
Search Non-Antibody Products
© 1980 - 2012 Linscott's Directory, Linscott's USA. All rights reserved.