Transformation of Bacteria: Difference between revisions

removed confusing buffer addition
updated transformation protocol
 
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==Materials==
==Materials==
*Competent Cells
*Competent Cells
*Plasmid amplification use subcloning efficiency DH5a
*SOC Buffer or LB Media
*Cloning use OneShot TOP10 (Pink)
*Mutagenesis use XL1 Blue Supercompetent (Blue), comes in 50uL aliquots
*SOC Buffer
*DNA of interest (1 uL for plasmid, 5 uL for cloning/mutagenesis)
*DNA of interest (1 uL for plasmid, 5 uL for cloning/mutagenesis)
*Plates (Amp or Kan; in cold room)
*Plates (Amp or Kan; in cold room, see [[ Making LB Agar Plates ]])


==Protocol==
==Protocol==