Electroblotting
![](http://upload.wikimedia.org/wikipedia/en/thumb/4/42/Electroblot.gif/300px-Electroblot.gif)
Electroblotting is a method in molecular biology/biochemistry/immunogenetics to transfer proteins or nucleic acids onto a membrane by using PVDF or nitrocellulose, after gel electrophoresis.[2][3] The protein or nucleic acid can then be further analyzed using probes such as specific antibodies, ligands like lectins, or stains. This method can be used with all polyacrylamide and agarose gels. An alternative technique for transferring proteins from a gel is capillary blotting.
Development
This technique was patented in 1989 by William J. Littlehales under the title "Electroblotting technique for transferring specimens from a polyacrylamide electrophoresis or like gel onto a membrane.[1][4]
Electroblotting procedure
This technique relies upon current and a transfer buffer solution to drive proteins or nucleic acids onto a membrane. Following electrophoresis, a standard tank or semi-dry blotting transfer system is set up. A stack is put together in the following order from cathode to anode: sponge | three sheets of filter paper soaked in transfer buffer | gel | PVDF or nitrocellulose membrane | three sheets of filter paper soaked in transfer buffer | sponge. It is a necessity that the membrane is located between the gel and the positively charged anode, as the current and sample will be moving in that direction. Once the stack is prepared, it is placed in the transfer system, and a current of suitable magnitude is applied for a suitable period of time according to the materials being used.
Typically the electrophoresis gel is stained with Coomassie brilliant blue following the transfer to ensure that a sufficient quantity of material has been transferred. Because the proteins may retain or regain part of their structure during blotting they may react with specific antibodies giving rise to the term immunoblotting. Alternatively the proteins may react with ligands like lectins giving rise to the term affinity blotting.
See also
- Western blotting
- SDS-page
References
- ^ a b R C Dubey (2014). Advanced Biotechnology. S. Chand Publishing. pp. 199–. ISBN 978-81-219-4290-4.
- ^ David Sheehan (30 April 2013). Physical Biochemistry: Principles and Applications. John Wiley & Sons. pp. 206–. ISBN 978-1-118-68748-2.
- ^ M. P. Bansal (1 January 2013). Molecular Biology and Biotechnology: basic experimental protocols. The Energy and Resources Institute (TERI). pp. 141–. ISBN 978-81-7993-379-4.
- ^ "United States Patent 4840714". Archived from the original on 2007-09-29. Retrieved 2007-05-24.
External links
- Protein (Western) Blotting - Introduction to Antibodies Membrane Transfer
- Detailed electroblotting to PVDF procedure - Protein Chemistry Laboratory
- v
- t
- e
- Protein purification
- Green fluorescent protein
- Western blot
- Protein immunostaining
- Protein sequencing
- Gel electrophoresis/Protein electrophoresis
- Protein immunoprecipitation
- Peptide mass fingerprinting/Protein mass spectrometry
- Dual-polarization interferometry
- Microscale thermophoresis
- Chromatin immunoprecipitation
- Surface plasmon resonance
- Isothermal titration calorimetry
- X-ray crystallography
- Protein NMR
- Cryo-electron microscopy
- Freeze-fracture electron microscopy