Team:NYMU-Taipei/Notebook




JUNE

week1

  1. Plasmid pET32a was extracted from competent cell BL21 DE3.
  2. We prepared competent cell solution buffer and made competent cell DH5-alpha.

JULY

week2

FRET MODEL

CELL MODEL

  1. Plasmid pUC19 was transformed into competent cell DH5-alpha.
  2. Plasmid pUC19 was extracted from competent cell DH5-alpha and checked by gel electrophoresis.
  3. Plasmid pUC19 was checked with restriction digestion(DpnI, EcoRI and BamHI).

week3

FRET MODEL

CELL MODEL

  1. Dkk1 promoter was amplified from HEK293 genomic DNA by KOD and DreamTaq polymerase PCR.
  2. DKK1 promoter PCR amplification checked by running an agarose gel(PCR failed).
  3. DH5-alpha pUC19 was stored in glycerol stock.

week4

FRET MODEL

week5

FRET MODEL

CELL MODEL

  1. KOD and DreamTaq polymerase PCR amplification of Dkk1 promoter from HEK293 genomic DNA.
  2. DKK1 promoter PCR amplification checked by running an agarose gel(Dream Taq success,KOD failed).
  3. troubleshooting of DKK1 promoter PCR amplification.
  4. KOD and DreamTaq polymerase PCR amplification of Dkk1 promoter from HEK293 genomic DNA.
  5. DKK1 promoter PCR amplification checked by running an agarose gel(Dream Taq success, KOD success).

AUGUST

week6

FRET MODEL

CELL MODEL

week7

FRET MODEL

CELL MODEL

week8

FRET MODEL

CELL MODEL

week9

FRET MODEL

CELL MODEL

SEPTEMBER

week10

FRET MODEL

CELL MODEL

week11

FRET MODEL

CELL MODEL

week12

FRET MODEL

CELL MODEL

week13

FRET MODEL

CELL MODEL

OCTOBER

week14

FRET MODEL

CELL MODEL

week15

FRET MODEL

CELL MODEL

week16

FRET MODEL

CELL MODEL