The technique is used to detect specific proteins from a tissue extract; Western blots can also be used to evaluate the size of a protein of interest, and to measure the quantity of protein expression.
From here, the first phase is known as the transfer step, what happens here is the movement of the proteins from solution to a biosynthetic membrane structure to form the 'blot'.
The second stage uses a treatment which is known as blocking, this stage inhibits any non-specific reactions from taking place. following this, the membrane is incubated with an antibody known as the primary antibody which binds to the protein of interest. After this, any unbound primary antibody is washed away, and the membrane is incubated once again, however this time with a secondary antibody that specifically recognises and binds to the primary antibody. The secondary antibody is linked to a reporter enzyme that produces colour allowing it to be easily detected and imaged.
- ↑ Serotec, A. (2015). Western Blot | What is Western Blotting?. [online] AbD Serotec. Available at: https://www.abdserotec.com/western-blotting.html [Accessed 2 Dec. 2015].
- ↑ Towbin H, Staehelin T, Gordon J. (1979). "Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications". Proceedings of the National Academy of Sciences USA 76 (9): 4350–54. doi:10.1073/pnas.76.9.4350. PMC 411572. PMID 388439.
- ↑ Bio-rad.com, (2015). Western Blotting | Applications &amp;amp;amp;amp; Technologies | Bio-Rad. [online] Available at: http://www.bio-rad.com/en-uk/applications-technologies/western-blotting [Accessed 2 Dec. 2015].
- ↑ Nature.com, (2015). Western blot | Learn Science at Scitable. [online] Available at: http://www.nature.com/scitable/definition/western-blot-288 [Accessed 2 Dec. 2015].