Materials

• Suspend the sample in buffer 1 (1.5 ml sample tube)
• Add buffer 2 to the sample and mix it
• Add buffer 3 to the sample and mix it
• Centrifuge for 5 minutes at 13,000 rpm and apply the supernatants to the column
• Add buffer 4 and centrifuge for 1 minute at 13,000 rpm then throw away the filter paper
• Add buffer 5 and centrifuge for 1 minute at 13,000 rpm then throw away the filter paper
• Centrifuge again for 1 minute at 13,000 rpm
• Place the column on a new sample tube and add 100 microL distilled water
• Centrifuge for 1 minute at 6,000 rpm

Materials

• Add buffer, dNTP, primer mix, Template DNA, KOD-FX-NEO and distilled water to an Eppendorf tube and mix
• Place the PCR tubes into the PCR machine and set the program

Materials

• Add buffer, dNTP, primer mix, Template DNA, KOD-FX-NEO and distilled water to an Eppendorf tube and mix
• Place the PCR tubes into the PCR machine and set the program

Materials

• Add all materials to a tube and mix them gently
• Incubate at 37˚C for the enzyme reaction for 15 minutes

Materials

• Set an agarose gel on an electrophoresis chamber
• Add 1X TAE buffer to the electrophoresis chamber
  Note: Do not generate bubbles under the gel
• Add 2X loading buffer to electrophoresis samples
• Apply samples on agarose gel wells
• Set an appropriate voltage (100 V) and run the electrophoresis
• Stop the electrophoresis when the BPB reaches 2/3 of the gel
• Soak the gel in EtBr (ethidium bromide) solution and dye it for 20 minutes
• Place plastic cooking wrap on the trans-illuminator and irradiate UV to the gel on the wrap
• Take photographs of the gel by using a trans-illuminator

Materials

• Add materials (DNA, H2O, CH3COONa, and Phe/Chl) to sample tube and vortex
• Centrifuge at 14,500 rpm for 10 minutes at room temperature
• Transfer the supernatant to a new sample tube
• Add 750 μL of isopropyl alcohol to the sample tube and vortex
• Centrifuge at 14,500 rpm for 10 minutes at 4°C
• Remove isopropyl alcohol gently so that the pellet will not break
• Add 1,000 μL of 75% ethanol and centrifuge at 14,500 rpm for 5 minutes at 4°C
• Dry it by aspirator for 10 minutes
• Add 25 μL of distilled H2O and mix

• Phe/Chl composition Phenol:Chloroform:Isoamyl alcohol=25:24:1

Materials

• Mix DNA sample and DNA ligase in a sample tube gently
• Ligation for 15 minutes at room temperature

Materials

• Thaw the competent cells on ice
• Add 10 μL of sample into thawed competent cells
• Cool the sample tube, which contains competent cells and DNA samples, with ice for 1 hour, then Heat shock the cells by immersion in pre-hearted water bath at 42°C for 30 seconds
• Place the tube on ice for 2 minutes to cool it down
• At a clean bench, add 1.0 ml of LB medium into the tube and suspend it
• Incubate the tube at 37°C for 35 minutes
• Harvest the cells by centrifuge
• Spread the transformed competent cells onto the agar plate and incubate it at 37°C overnight

Materials

• Scrape samples from the agar plate and inoculate them on medium
• Cultivate at 37°C in a shaken culture overnight

Materials

• Scrape samples from the agar plate and inoculate them in liquid media
• Cultivate overnight (37˚C, 120 rpm)

Materials

• Separate samples into two and harvest by centrifuge
• Add potassium phosphate buffer, then mix and remove medium completely
• Add Fast Break Cell Lysis Reagent, 10X at the ratio of Fast Break Buffer Cell Lysis Reagent,10X: Samples=1:9 and extract protein for 15 minutes at room temperature

Materials

• Harvest yeast cells by centrifuge at 3,000 rpm for 4 minutes at room temperature
• Wash cells once with potassium phosphate buffer
• Cool down the sample tube on ice for 1 minute
• Add the same amount of glass beads as the sample then add 20 μL of potassium phosphate buffer and mix
• Disrupt the cells by FastPrep 24 (MP Biochemicals) for 45 seconds at speed 4.5
• Cool down the sample tube on ice for 1 minute
• Add 80 µl of potassium phosphate buffer, cool it down and centrifuge for 5 minutes at 14,500 rpm at 4°C
• Transfer 40 µl of the supernatant and mix with 8 µl of SDS sample buffer
• Treat the sample with heat for 5 minutes at 100˚C

Materials

• Dispense cracking solution (50 μL) each into sample tubes
• Collect the sample and suspend it into cracking solution
• Incubate at 65°C for 10 minutes
• Add Phe/Chl and BPB pigment and vortex
• Centrifuge at 14,000 rpm for 5 minutes
• Apply the samples (upper layer) to agarose gel with loading dye
• Check the bands by agar gel electrophoresis

Materials

• Place stacking gel on separating gel
• Rinse the wells of gel with distilled water
• Load prepared samples into wells
• Run the electrophoresis (25 mA for 75 min)
• Check the bands with CBB stain

Materials

• Cut the gel in appropriate size
• Add BufferⅢ and gel then shake it gently
• Soak the membrane on ethanol then soak it in BufferⅢ and percolate
• 2, 1, 3 Whatman papers (all in the same size) on BufferⅠ, BufferⅡ, BufferⅢ respectively. wet the surface of the blotter
• Blot at the constant current of membrane's area ×2.5 mA
• Dye the membrane with Ponceau S for 5 minutes rinse it with distilled water and scan it
• Shake and wash with PBS-TS (3 minutes ×3 times)
• Put the membrane in a hybridization bag add PBS-S antiglutathione S-transferase and shake it for one hour at room temperature
• Shake and wash with PBS-T twice (5 min/10 min)
• Shake and wash with PBS twice (5 min/5 min)
• Add one drip of 3 Peroxidase Stain Kits and distilled water
• Scan it

• BufferⅠ: bring to 300 ml with Tris base 10.9g, MetOH60ml/H2O
• BufferⅡ: bring to 300 ml with Tris base 0.9g, MetOH60ml/H2O
• BufferⅢ: bring to 300 ml with Tris base 0.91g, Boric acid10.5mg, MetOH60ml/H2O
• PBS-S: PBS with 1% SkimMilk
• PBS-T: PBS with 0.05% Tween20
• PBS-TS: PBS with 0.05% Tween20+1% SkimMilk

Materials

• Dissolve Tryptone (1.0 g), Yeast Extract (500 mg) and NaCl (1.0 g) in distilled water (90 ml)
• Adjust pH to 7.0 by adding 20μL of 5M NaOH
• Fill up to 100 ml with distilled water
• Autoclave

• To make agar plate, add agar powder at the final concentration of 2 %(w/v) in Procedure 2

• Dissolve peptone (2.0 g), yeast extract (1.0 g) and glucose (2.0 g) to distilled water (90 ml)
• Fill up to 100 ml with distilled water
• Sterilize by autoclave

• To make agar plate, add agar powder (final concentration: 2.0%) at procedure 1.

Materials

• Dissolve yeast nitrogen base (6.7 g), adenine (40 mg), histidine (20 mg), leucine (60 mg), lysine (30mg), tryptophan (40mg) and methionine (20mg) into 40 ml of distilled H2O, and then fill up to 50 ml with H2O.
• Dissolve glucose (20.0 g) into 40 ml of distilled H2O, and then fill up to 50 ml with H2O.
• Sterilize each solution by autoclave.
• Mix solutions after cooling it down.

• Autoclave glucose and agar plate separately from other materials