Detection of GST-tagged Proteins with Western Blot
Expression and purification of GST-tagged proteins can be monitored by Western blot analysis, using Amersham ECL, Amersham ECL Prime, or Amersham ECL Select detection systems to enhance sensitivity.
Secondary antibody to detect the anti-GST antibody (such as anti-goat IgG HRP conjugate)
Appropriate membrane, such as Amersham Hybond™ ECL (nitrocellulose) or Amersham Hybond-P (PVDF)
Electrophoretic Separation of Proteins
- Separate the protein samples by SDS-PAGE.
Although anti-GST antibody from Cytiva has been cross-adsorbed with E. coli proteins, low levels of cross-reacting antibodies may remain. Samples of E. coli lysates that do not contain a recombinant pGEX plasmid and samples that contain the parental pGEX plasmid should always be run as controls.
- Transfer the separated proteins from the electrophoresis gel to the membrane.
Electrophoresis and protein transfer can be accomplished using a variety of equipment and reagents.
Blocking of Membrane
- Transfer the membrane onto which the proteins have been blotted into an appropriately sized container, such as a Petri dish.
- Add 50 to 200 mL of blocking/incubation buffer to the container.
- Incubate with agitation for 1 h at room temperature, or at 37 °C if the background is persistently and unacceptably high. Alternatively, membranes may be left in the blocking solution overnight at 2 °C to 8 °C, if more convenient.
- Decant and discard the buffer.
- Briefly rinse the membrane in wash buffer.
Longer incubation times with blocking/incubation buffer may reduce background signal.
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