I am treating cultured AVCMs from mice and analyzing gene expression with a collaborator. Normally, I would just isolate the total RNA from the culture wells and perform PCR. In this specific case, I need to ship either the cardiomyoctyes or the extracted RNA to a collaborator. If I extract the RNA then I need to freeze and ship frozen samples. Less than ideal.
My other option is to put the cardiomyoctyes in RNAlater. If we use RNAlater, would you scrape the cardiomyoctyes in RNAlater or trypsinize, pellet and resuspend them in RNAlater? I have never had a need to trypsinize primary cardiomyoctyes before and scraping primary cardiomyoctyes seems a bit aggressive. If I recall we had a bit of an issue getting a cell pellet (HL-1 cells) out of RNAlater in the past.
Any suggestions are appreciated...