Team:HokkaidoU Japan/Protocols

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HokkaidoU_Japan Protocols

  • Preparation of Competent cells (E. coli DH5a)

    Reagents

    TB (Transformation Buffer)(at 4C, filtration)

    Final concentration
    1 M CaCl2 (at RT, autoclaved) 0.75 mL 15 mM
    4 M KCl (at RT, autoclaved) 3.125 mL 250 mM
    1 M MnCl2 (at 4C, autoclaved) 2.75 mL 55 mM
    1 M PIPES (pH 6.7 by NaOH, at 4C, filtration) 0.5 mL 10 mM
    Total 50 mL

    Procedure

    1. Single colony isolation on LB plate
    2. Incubate the plate for 15-19 hrs at 37C
    3. Lift a colony into 2 mL of LB
    4. Culture cells at 37C for 12-16 hrs at 180-200 rpm
    5. Transfer 30 uL, 100 uL, 300 uL of the culture into 100 mL SOB medium, respectively
    6. Culture cells at 20C (for 24 hrs over) at 180-200 rpm (to ΔOD550nm = 0.5~0.6)
    7. Leave the 300 mL flask for 10 min on ice
    8. Transfer the culture into two 50 mL Falcon tube
    9. Centrifuge 7500 rpm at 4C for 20 min (TOMY TA-22 rotor), and discard sup
    10. Suspend the pellet in ice-cold 15 mL of TB (Transformation Buffer)(7.5 mL/tube)
    11. Centrifuge 7500 rpm at 4C for 2 min (TOMY TA-22 rotor), and discard sup
    12. Suspend the pellet in ice-cold 3.2 mL of TB
    13. Add 0.24 mL of DMSO (stirring, bit by bit)
    14. Leave the 50 mL Falcon tube for 10 min on ice
    15. Dispense 50 uL into 0.5 mL tube
    16. Freeze the suspension in liquid nitrogen
    17. Store at -80C

  • Bacterial Transformations

    1. Add DNA solution to thawed competent cells
    2. Incubate the cells on ice for 30 min
    3. Heat shock the cells by immersion in a pre-heated water bath at 42C for 60 sec
    4. Incubate the cells on ice for 5 min
    5. Add 200 uL of SOB broth
    6. Incubate the cells at 37C for 2 hrs while the tubes are shaking
    7. Plate 200 uL of the transformation onto the dish
    8. Incubate the plate at 37C for 12-14 hrs

  • Mini-prep (Alkaline SDS Method)

    Reagents

    Solution I (at RT, filtration 0.2 um, 50 mL)

    Final concentration
    Glucose (at RT) 0.45 g 50 mM
    1 M Tris-HCl (pH8.0, at RT, autoclaved) 1.25 mL 25 mM
    0.5 M EDTA (pH8.0, at RT, autoclaved) 1 mL 10 mM
    Total 50 mL


    Solution II (at RT, filtration 0.2 um, 20 mL)

    Final concentration
    10 N NaOH (at RT) 0.4 mL 0.2 N
    10% SDS (at RT, filtration) 2 mL 1%
    Total 20 mL


    Solution III (at RT, filtration 0.2 um, 50 mL)

    Final concentration
    5 M CH3COOK 30 mL 3 M
    CH3COOH 5.75 mL
    H2O 14.25 mL
    Total 50 mL

    Procedure

    1. Lift colony E. coli into 2 mL LB contained antibiotics
    2. Culture cells at 37C for 16-20 hrs at 180-200 rpm
    3. Transfer 1.2-1.5 mL of culture into 1.5 mL tube
    4. Centrifuge the culture at 15,000 rpm for 1 min at 4C and discard sup
    5. Suspend the pellet in ice-cold 100 uL of Solution I
    6. Add 200 uL of Solution II to the suspension
    7. Mix by inverting the tube 10-20 times
    8. Add ice-cold 150 uL of Solution III to the suspension
    9. Mix by inverting the tube 10-20 times
    10. Leave the tube for 5 min on ice
    11. Add 10 uL of Chloroform
    12. Mix by inverting the tube 5-10 times
    13. Centrifuge the suspension at 15,000 rpm for 5 min at 4C
    14. Transfer the supernatant into new 1.5 mL tube↓
    15. Add equal volume of isopropanol and mix by voltexing
    16. Leave the tube for 5 min at RT
    17. Centrifuge the suspension at 15,000 rpm for 10 min at 4C and discard sup
    18. Rinse the ppt by 70% EtOH and mix by voltexing
    19. Centrifuge the suspension at 15,000 rpm for 2 min at 4C and discard sup
    20. Dry up the ppt
    21. Dissolve the ppt in 50 uL of TE (pH 8.0)
    22. Add 1 uL of 10 mg/mL RNase A (4C and stock at –20C)
    23. Incubate for 30 min at 37C
    24. PCIAA and CIAA extraction
    25. Ethanol precipitation
    26. Dry up the ppt
    27. Dissolve the ppt in 50 uL of TE (pH 8.0)

  • PCR

    Vector

    Standard reaction setup

    Component Volume
    10x PCR Buffer 5 uL
    2mM dNTPs 5 uL
    25mM MgSO4 3 uL
    Suffix-F primer 1 uL
    Prefix-R primer 1 uL
    Template DNA 1 uL
    KOD -Plus- Neo 1 uL
    DW X uL
    Total 50 uL

    Cycling conditions (2-step cycle)

    Predenature 94C 2 min
    Denature 98C 10 sec
    Extension 68C X sec (30 sec/kb)
    Hold 4C
    • 30-40 cycles

    Insert

    Standard reaction setup

    Component Volume
    10x PCR Buffer 5 uL
    2mM dNTPs 5 uL
    25mM MgSO4 3 uL
    EX-F primer 1 uL
    PS-R primer 1 uL
    Template DNA 1 uL
    KOD -Plus- Neo 1 uL
    DW X uL
    Total 50 uL

    Cycling conditions (2-step cycle)

    Predenature 94C 2 min
    Denature 98C 10 sec
    Extension 68C X sec (30 sec/kb)
    Hold 4C
    • 30-40 cycles

    Colony PCR

    • resuspend a colony into 10 uL of DW (template suspension)

    Standard reaction setup

    Component Volume
    template suspension 4.8 uL
    Quick Taq 5 uL
    Forward primer 0.1 uL
    Reverse primer 0.1 uL
    Total 10 uL

    Cycling conditions (2-step cycle)

    Predenature 94C 2 min
    Denature 94C 10 sec
    Extension 68C X sec (60 sec/kb)
    Hold 4C
    • 30-40 cycles

  • Restriction Enzyme Digestions

    c

  • DNA ligation

    d

  • Agarose gel electrophoresis

    DNA Weight Markers

  • Electroporation

    Preparation of electro-competent cells

    1. Cell culture in 400 mL of SOB or LB and grow to ΔOD600 = 0.5~0.6
    2. Dispense the medium into 8 Falcon 50 mL tube
    3. Centrifuge at 3500 rpm for 5 min at 4C and discard sup
    4. Add 5 mL of DW and suspend the ppt, mix 8 suspensions into single Falcon tube
    5. Centrifuge at 3500 rpm for 5 min at 4C and discard sup
    6. Add 40 mL of DW and suspend the ppt
    7. Centrifuge at 3500 rpm for 5 min at 4C and discard sup
    8. Add 10 mL of 10% Glycerol and suspend the ppt
    9. Centrifuge at 3500 rpm for 5 min at 4C and discard sup
    10. Add 10 mL of 10% Glycerol and suspend the ppt
    11. Centrifuge at 3500 rpm for 5 min at 4C and discard sup
    12. Add 5 mL of 10% Glycerol and suspend the ppt
    13. Dispense 100 uL of the suspensions into 0.5 mL Eppendorf tube, respectively
    14. Store at -80C freezer


    Electroporation

  • PCIAA and CIAA extraction

    Reagent

    • PCIAA = Phenol : CIAA = 1 : 1
    • CIAA = Chloroform : IsoAmyl Alcohol = 24 : 1

    Procedure

    1. Add equal volume of PCIAA and vortex vigorously
    2. Centrifuge at 15,000 rpm for 2 min at RT
    3. Transfer the aqueous phase to a new tube, being careful not to transfer the phase interface
    4. Add equal volume of CIAA and vortex vigorously
    5. Transfer the aqueous phase to a new tube
    6. Ethanol precipitation


  • Ethanol presipitation

    1. Add 1/10 volume of 3M CH3COONa
    2. Add 2.5 volume of 100% ethanol (EtOH)
    3. Incubate on ice for few min
    4. Centrifuge at 15,000 rpm for 10 min at 4C and discard sup
    5. Wash precipitation with 100 uL of 70% EtOH (EtOH has to be cold)
    6. Centrifuge at 15,000 rpm for 5 min at 4C and discard sup
    7. Dry up the ppt (no EtOH should be left)
    8. Resuspend ppt in wanted volume of TE

  • Mini-prep (QIAprep Spin Miniprep Kit)

    1. Resuspend pelleted bacterial cells in 250 µl Buffer P1 and transfer to a micro-centrifuge tube
    2. Add 250 µl Buffer P2 and mix thoroughly by inverting the tube 4–6 times
    3. Add 350 µl Buffer N3 and mix immediately and thoroughly by inverting the tube 4–6 times
    4. Centrifuge for 10 min at 13,000 rpm (~17,900 x g) in a table-top microcentrifuge
    5. Apply the supernatants from step 4 to the QIAprep spin column by decanting or pipetting
    6. Centrifuge for 30–60 s. Discard the flow-through
    7. Recommended: Wash the QIAprep spin column by adding 0.5 ml Buffer PB and centrifuging for 30–60 s. Discard the flow-through
    8. Wash QIAprep spin column by adding 0.75 ml Buffer PE and centrifuging for 30–60 s
    9. Discard the flow-through, and centrifuge for an additional 1 min to remove residual wash buffer
    10. Place the QIAprep column in a clean 1.5 ml microcentrifuge tube. To elute DNA, add 50 µl Buffer EB (10 mM Tris·Cl, pH 8.5) or water to the center of each QIAprep spin column, let stand for 1 min, and centrifuge for 1 min
    • [http://www.qiagen.com/products/plasmid/qiaprepminiprepsystem/qiaprepspinminiprepkit.aspx see details (Official website)]

  • Gel Extraction (Wizard® SV Gel and PCR Clean-Up System)

    1. Following electrophoresis, excise DNA band from gel and place gel slice in a 1.5 mL microcentrifuge tube
    2. Add 10 uL Membrane Binding Solution per 10 mg of gel slice
    3. Vortex and incubate at 50–65C until gel slice is completely dissolved
    4. Insert SV Minicolumn into Collection Tube
    5. Transfer dissolved gel mixture or prepared PCR product to the Minicolumn assembly
    6. Incubate at room temperature for 1 min
    7. Centrifuge at 16,000 g for 1 min
    8. Discard flowthrough and reinsert Minicolumn into Collection Tube
    9. Add 700 uL Membrane Wash Solution (ethanol added)
    10. Centrifuge at 16,000 g for 1 min
    11. Discard flowthrough and reinsert Minicolumn into Collection Tube
    12. Repeat Step 4 with 500 uL Membrane Wash Solution
    13. Centrifuge at 16,000 g for 5 min
    14. Empty the Collection Tube and recentrifuge the column assembly for 1 min with the microcentrifuge lid open (or off) to allow evaporation of any residual ethanol
    15. Carefully transfer Minicolumn to a clean 1.5 mL microcentrifuge tube
    16. Add 50 uL of Nuclease-Free Water to the Minicolumn
    17. Incubate at room temperature for 1 min
    18. Centrifuge at 16,000 g for 1 min
    19. Discard Minicolumn and store DNA at 4C or –20C
    • [http://www.promega.com/applications/pcr/featuresandbenefits/Wizard_SV_Gel_PCR_Clean-Up_System.htm see details (Official website)]

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