Western blotting or immunoblotting is an indispensable technique, almost every published paper in area of molecular cell biology uses western blotting for detecting specific proteins in a sample of tissue homogenate or cell lysates. Western blotting combines resolving power of polyacrylamide gel electrophoresis (PAGE) or SDS-PAGE and specificity of antibodies to detect target proteins. Proteins are resolved on the basis of their molecular weight in SDS-PAGE and transferred from the polyacrylamide gel onto the membranes (Nitrocellulose or PVDF), which creates an exact replica of the protein separation pattern on the membrane. After transferring the proteins to the membrane, the membrane needs ‘blocking’ to ‘block’ non-specific binding sites on the surface of the membrane. Blocking is usually performed with Bovine Serum Albumin, Skimmed milk or purified milk Casein.
Topics: Protein Purification, Western Blotting, Protein Electrophoresis, Protein Estimation, Sample Clean Up, Protease Inhibitors, Protein Extraction, Protein Detection
His-tagged protein expressing but not binding your Ni-NTA column?
Poly-histidine tagged proteins account for more than 90% of routine recombinant protein expression and purification. Histidine tag has many advantages over other affinity tags such as small size, high affinity for binding to IMAC resins (Immobilized metal affinity chromatography) and allows one step purification of recombinant protein. But sometimes a histidine tagged protein doesn’t bind to the affinity column and evades it’s capture and subsequent purification. Although such instances are not very common but can be very frustrating whenever they happen. However, there are ways to troubleshoot if such a problem arises and the solutions are discussed below in a step by step manner.
Topics: Protein Purification, Western Blotting, Protein Electrophoresis, Sample Clean Up, Protein Concentration, Protein Fractionation, Protein Labeling, Protein Extraction, Protein Detection
Cysteine is one of the most reactive amino acid residue owing to the thiol (-SH) group, thiols can serve as an electron donor in different reactions. Cysteine thiols can form part of catalytic centre and can frequently participate in enzymatic reactions, not just that, cysteine thiols can also undergo a variety of covalent post-translational modifications (PTMs) and formation of disulphide bonds. The thiol modifications can act as important mediators of redox signalling and protein function regulation.
Topics: Protein Purification, Protein Electrophoresis, Sample Clean Up, Protein Extraction