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I have different sizes of Fc fusion plasmids, I transfected with 293T cells and purified with protein A beads. After that, I run the protein gel and found that they showed the same bands. But If...
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I plan to do the CRISPR-cas9 base edit in mouse cells, it is better to use the primary cells or immortalized cell lines? I have read some papers, some used the primary cell lines.
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