Monoclonal antibodies are derived from a single immortal B-cell line. Thus, monoclonal antibodies can only recognize one single epitope on your antigen.
How to dilute antibodies?
In contrast, polyclonal antibodies are derived from the serum collected from animals exposed to the antigen. Thus, polyclonal antibodies are in fact a collection of antibodies generated from many B cells.
Having trouble to find the dilution ratio for your antibody? Try out Antibody Dilution Bank
When cells are infected, our innate immunity produces Interferon. Interferon stimulates the transcription of interferon stimulated genes (ISGs). One of the ISGs is called the 2-5A synthetase. 2-5A synthetase senses dsRNA (converting ATP to 2-5A), which in turns activates RNaseL. Activated RNaseL then cleaves ssRNA regardless of cellular or viral origin.
How can virus counteract the host’s response? Vaccinia virus and reovirus encodes a dsRNA binding protein to sequester the exposure of dsRNA from 2-5A synthetase.
Making Agar Plate
20g LB Broth
15g Bacto Agar
Mix well first. Pour the mixture into a 2L flask.
Some bacto agar will not be completely dissolved. Therefore, you can always let the bacto agar to settle in your 2L flask, then take the top phase of liquid to flush the remaining bacto agar out.
After that, put it into autoclave machine (wet cycle: this is often preset. But usually it is 100C for 20-30 minutes)
If you wish to make plates for penicillin, wait until the flask to cool down a bit, don’t wait for too long, otherwise the agar will solidify (if you can bear the temperature with your bare skin, the temperature is good). At this time, add penicillin at 1:1000 dilution.
Making LB Broth
40 g LB Broth
Mix well, pour into 4 glass bottles, then autoclave
*When autoclaving liquid in glass bottles, make sure to not tighten the glass bottle completely.