Optimized conditions for cloning PCR products into an XcmI T-vector

Biotechniques. 1997 Jan;22(1):40-2, 44. doi: 10.2144/97221bm06.
No abstract available

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Sequence
  • Cloning, Molecular*
  • DNA Restriction Enzymes
  • DNA, Fungal / genetics
  • Genetic Vectors
  • Molecular Sequence Data
  • Polymerase Chain Reaction / methods*

Substances

  • DNA, Fungal
  • DNA Restriction Enzymes

Associated data

  • GENBANK/U61229