Materials

Materials

  1. PCR primer (invA)
  2. dNTPs (100mM each)
  3. Taq DNA polymerase (3 U/ml)
  4. PCR buffer with MgCl2
  5. Ethidium bromide (5 mg/μl)
  6. Agarose (2%) in 1X TAE
  7. 6 X Gel loading dye
  8. 1 X TAE buffer (pH 8.5)
    Dissolve 48.4g Tris base and 7.44 g Di-sodium EDTA in 1.42 ml glacial acetic acid and make upto 1000 ml with molecular grade water
Last modified: Saturday, 12 November 2011, 7:46 AM