Hello, my English is bad, please be considerate. Thanks!
I've been using the 3321-4AST for five months and have been having a problem with the high background of the unirritated well. Recently I've compiled past results and found that there has been a phenomenon that the background of the vaccine-immunized mice is significantly higher than that of the placebo-immunized mice. This has caused a lot of trouble for my experiment. I am new to immunology and have not found a good solution. I hope to get your help.
Seven days after the immunization, I removed the lungs of the mice, treated them with red blood cell lysate, and isolated the lung lymphocytes of the mice using procoll. For the culture, I used RPMI 1640 medium with 10% fetal bovine serum at 200,000 cells per well. In each trial, the vaccine-immunized mice had a higher background than the placebo-immunized mice, leading to fatal false negatives. Do you have any good suggestions for improvement?
I guess it may be because after immunization, there is some IFN γ in the differentiated lymphocytes of mice, which leads to the release of IFN γ even without any stimulation during the culture process. But I don't know whether IFN γ must be produced and released immediately, and whether IFN γ will be stored in the cytoplasm of differentiated lymphocytes? I have just come into contact with the knowledge of immunology, and I have not found the exact relevant literature. Do you know any knowledge in this regard?
Besides, I found that the intra- and inter-experiment reproducibility is very poor, which makes the experimental results unconvincing. Do you have any suggestions for improving the experimental reproducibility?
Looking forward to your reply, thank you very much.