Hello, Has anyone had any experience with cutting cell mixed with 2% low melting agarose gel? The cells were fixed in 10% NBF, mixed with the gel and then processed to a paraffin block.
I've tried a couple of techniques, but the end result is mush. Any ideas or suggestions? Bobbie Boyce Histology Specialist III duPont Hospital for Children Biomedicla Research, ARB 264 1600 Rockland Road Wilmington, DE 19803 302-651-6771 (Lab) 302-651-5010 (Fax) _______________________________________________ Histonet mailing list [email protected] http://lists.utsouthwestern.edu/mailman/listinfo/histonet
