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MABE1068 Sigma-AldrichAnti-APE/Ref-1 Antibody, clone 13B8E5C2
Anti-APE/Ref-1, clone 13B8E5C2, Cat. No. MABE1068, is a highly specific mouse monoclonal antibody, that targets APE1 and has been tested in Immunocytochemistry, Immunohistochemistry (Paraffin), and Western Blotting.
100069 Sigma-Aldrich17-DMAG - CAS 467214-21-7 - Calbiochem
17-DMAG, CAS 467214-21-7, is a more potent antitumor analog of 17-AAG (Cat. No. 100068) that binds to the ATPase site of human Hsp90α with high affinity (GI50 = 51 nM).
149101 Sigma-Aldrich1-Aminocyclopropane-1-carboxylic Acid - CAS 22059-21-8 - Calbiochem
1-Aminocyclopropane-1-carboxylic Acid - CAS 22059-21-8, is an agonist for the glycine modulatory site of the N-methyl-D-aspartate (NMDA) receptor complex.
531170 Sigma-AldrichALDH3A1 Inhibitor, CB29 - Calbiochem
A cell permeable, selective, reversible, substrate-binding site directed inhibitor of aldehyde dehydrogenase ALDH3A1 (Ki = 4.7 µM, IC₅₀ = 16 µM).
531492 Sigma-Aldrich12/15-Lipoxygenase Inhibitor, ML351 - CAS 847163-28-4 - Calbiochem
A cell-permeable, highly potent, selective, active site directed, mixed type inhibitor of lipoxygenase-12/15 (IC50 = 200 nM for human).
69439 Sigma-AldrichpET-11d DNA
Novagen's pET-11a-d vectors carry an N-terminal T7-Tag sequence and BamH I cloning site. The pET-21a-d(+) series corresponds to pET-11a-d but incorporates several additional features.
239831 MilliporeD-Cycloserine - CAS 68-41-7 - Calbiochem
D Cycloserine is a partial agonist of NMDA receptors at the glycine modulatory site. Reported to improve memory-dependent tasks in rats. Neutral and acidic solutions are unstable.
69436 Sigma-AldrichpET-11a DNA - Novagen
Novagen's pET-11a-d vectors carry an N-terminal T7-Tag sequence and BamH I cloning site. The pET-21a-d(+) series corresponds to pET-11a-d but incorporates several additional features.
69770 Sigma-AldrichpET-21(+) DNA - Novagen
Novagen's pET-21(+) is a transcription vector that lacks the ribosome binding site and ATG start codon present on the pET translation vectors.
208292 Sigma-AldrichL-Type Calcium Channel Blocker
A cell-permeable sulfonamide compound that reversibly interacts with the benzothiazepine-binding site and acts as a cardiac tissue selective L-type voltage gated Ca2+-channel activity inhibitor.