Buffers & Concentrates

ExpressPlus™ PAGE Gel,10×8, 8%, 12 wells,20Gels

ExpressPlus™ PAGE Gel,10×8, 8%, 15 wells,20Gels

ToxinEraser™ Regeneration Buffer,125ml

ToxinEraser™ Equilibration Buffer,125ml

5X Sample Buffer,5ml

Proprietary mixture including biotinylated and non-biotinylated NAD+, optimized for use with BPS Bioscience's poly(ADP) ribose polymerase (PARP) assay kits: PARP1 Chemiluminescent Assay Kit (BPS Bioscience #80551) PARP2 Chemiluminescent Assay Kit (BPS Bioscience #80552) PARP3 Chemiluminescent Assay Kit (BPS Bioscience #80553) PARP10 Chemiluminescent Assay Kit (BPS Bioscience #80560)

Proprietary mixture including biotinylated and non-biotinylated NAD+, optimized for use with BPS Bioscience's poly(ADP) ribose polymerase (PARP) assay kits: PARP6 Chemiluminescent Assay Kit (BPS Bioscience #80556) PARP7 Chemiluminescent Assay Kit (BPS Bioscience #79729) PARP11 Chemiluminescent Assay Kit (BPS Bioscience #80561) PARP14 Chemiluminescent Assay Kit (BPS Bioscience #80568)

BlockOut® Universal Blocking Buffer Solution for Western Blotting is specifically designed for colorimetric, chemiluminescent, and fluorescent western blotting. BlockOut® is recommended for blocking when phospho specific antibodies are used. Pure nitrocellulose membrane is recommended for maximum performance. Other membranes, such as PVDF or nitrocellulose embedded in a support can be used, but may generate elevated backgrounds. Protein should be transferred from gel to membrane using standard protocols. BlockOut® Blocking buffer can be used for membrane blocking and to dilute both primary and secondary antibodies. BlockOut® is suitable for use with chemiluminescent and fluorescent western blot imaging systems produced by Bio-Rad Laboratories, GE Healthcare, Alpha Innotech, FujiFilm Life Science, Licor Biosciences, UVP and Syngene.

Prepared by a modification of the method of Emanuel and Chaikoff, JBC 203, 164 (1953) from salmon testes DNA by mechanical shearing and heat denaturation to an average size of 100 to 200 base pairs. To reverse any renaturation occurring during storage, this material should be briefly boiled and rapidly chilled prior to use. >75% native nucleic acid.