proACE™ Blocking Solution is a blocking buffer for Western Blotting, ELISA and immunohistochemistry. It consists of high molecular weight compounds and bovine serum protein.
proACE™ ECL direct is ready-to-use enhanced luminol-based substrate for horseradish peroxidase (HRP) in chemiluminescent Western blotting assays. It allows for the detection of mid picogram amounts of HRP-conjugated antibodies, with long lasting signals (up to 3 hours)
proACE™ Green DNA Stain is a new and safe alternative to ethidium bromide (EtBr) for the visualization of DNA (double-stranded and single-stranded DNA) and RNA in agarose and polyacrylamide gels. The dye has been developed for in-gel staining and post-staining and is compatible with both UV and Blue LED transilluminators.
proACE™ Ultra ECL direct is ready-to-use enhanced luminol-based substrate for horseradish peroxidase (HRP) in chemiluminescent Western blotting assays. It allows for the detection of low femtogram amounts of HRP-conjugated antibodies, with long lasting signals (up to 2 hours)
Proteinase K is a broad-spectrum serine protease (28.9kDa monomer) that cleaves peptide bonds at the carboxylic sides of aliphatic, aromatic, and hydrophobic amino acids.
RNase A (Ribonuclease A) is a pancreatic endoribunuclease (13.7kDa monomer) that specifically cleaves single-stranded RNA at the 3′ end of pyrimidine residues.
RNase A (Ribonuclease A) is a pancreatic endoribunuclease (13.7kDa monomer) that specifically cleaves single-stranded RNA at the 3′ end of pyrimidine residues.
Ribonuclease A is a pancreatic endoribunuclease that specifically cleaves single-stranded RNA at the 3’ end of pyrimidine residues. Lyophilized powder purified from bovine pancreas
Ready-to-use solution, supplied in an easy-to-use Spray Bottle, for eliminating RNase, DNase, and other enzymes, as well as DNA contamination, from laboratory surfaces and material. Simply spray on the contaminated area and wipe away from the surface using ultrapure water.
Heat-labile multipurpose alkaline phosphatase that catalyzes the dephosphorylation of DNA, RNA and nucleotides. This recombinant enzyme replaces native SAP because it is much more stable at room temperature and is available at higher concentrations.