I have several questions regarding methods, kits, etc. Any help is
appreciated:
1) Suggested reference (or personal experience) for using PCR to
sequence, when the template is bacterial genomic DNA.
2) Fluorscent tagging of PCR products, either in the primer or in
precursors (or both).
3) How long a non-homologous 5' tail can be put on a PCR primer?
