I'm currently working with carcinoma model in Balb/C mice and particularly with C-26 cell line. I have a general question - some people induce solid tumor development by injecting C-26 cell in the mice and other prefer transplantation of part of existing tumor from other animal. What is the difference. I use cell suspension for this and have some good results, but I need to know if there is an important difference and to correct my method in such case.
Thanks in advance!
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C-26 tumor model in Balb/C
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