The Bicinchoninic Acid (BCA) Protein Assay, also known as the Smith Assay, is a highly sensitive colorimetric assay that is compatible with detergent solubilized protein solutions. The Bicinchoninic Acid (BCA) Protein Assay primarily relies on two
The Bicinchoninic Acid (BCA) Protein Assay, also known as the Smith Assay, is a highly sensitive colorimetric assay that is compatible with detergent solubilized protein solutions. The Bicinchoninic Acid (BCA) Protein Assay primarily relies on two
Following in gel digestion of proteins with proteases, the addition of Pep-Extract &trade rapidly elutes digested peptides in under 20 minutes. The eluted peptides can be used directly in mass spectrometry analysis, without any additional clean up.
Following in gel digestion of proteins with proteases, the addition of Pep-Extract &trade rapidly elutes digested peptides in under 20 minutes. The eluted peptides can be used directly in mass spectrometry analysis, without any additional clean up.
Protein-OUT&trade is a unique washing solution that cleans plastic and glassware used in the proteolytic digestion and peptide isolation for mass spectrometry analysis. The rinsing of plastic and glassware with Protein-OUT&trade will remove
Protein-OUT&trade is a unique washing solution that cleans plastic and glassware used in the proteolytic digestion and peptide isolation for mass spectrometry analysis. The rinsing of plastic and glassware with Protein-OUT&trade will remove
Proteomics often involves the purification and identification of novel proteins from tissues.  The strategy often employed is one using multiple and different protein purification techniques to fractionate proteins into specific fractions.
Proteomics often involves the purification and identification of novel proteins from tissues.  The strategy often employed is one using multiple and different protein purification techniques to fractionate proteins into specific fractions.
Molecular cloning is a commonly used technique for the generation of recombinant proteins.  The gene for a protein of interest is cloned into a vector, or plasmid, in frame with the gene for a protein tag.
Molecular cloning is a commonly used technique for the generation of recombinant proteins.  The gene for a protein of interest is cloned into a vector, or plasmid, in frame with the gene for a protein tag.
The cellular environment is a constant dynamic with the continued synthesis, degradation and recycling of protein molecules.  This dynamic allows for close regulation of cellular processes by switching off cellular pathways by degrading key
The cellular environment is a constant dynamic with the continued synthesis, degradation and recycling of protein molecules.  This dynamic allows for close regulation of cellular processes by switching off cellular pathways by degrading key
A form of LPS extracted from wild-type S-form E. coli serotype O113:H10 prepared to effectively remove traces of protein and nucleic acid while maintaining a consistently high concentration of endotoxin units.
A form of LPS extracted from wild-type S-form E. coli serotype O113:H10 prepared to effectively remove traces of protein and nucleic acid while maintaining a consistently high concentration of endotoxin units.
bio-WORLD's immunoaffinity columns will remove many of the abundant proteins in serum that interfere with proteomic analysis. These include albumin, transferrin, haptoglobin, alpha-1-antitrypsin, and many of the immunoglobins.
bio-WORLD's immunoaffinity columns will remove many of the abundant proteins in serum that interfere with proteomic analysis. These include albumin, transferrin, haptoglobin, alpha-1-antitrypsin, and many of the immunoglobins.