Knockout1

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(Procedure)
(Procedure)
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**Electroporator
**Electroporator
-
==== Procedure ====
+
==== '''Procedure''' ====
*'''Preparation of plasmids'''
*'''Preparation of plasmids'''
# Grow up pKD46, pKD13, and pCP20 in proper host strains
# Grow up pKD46, pKD13, and pCP20 in proper host strains
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| align="center" style="background:#FFFACD;"|'''Vol.'''
| align="center" style="background:#FFFACD;"|'''Vol.'''
|-
|-
-
| pKD13 template||45 ng/㎕||1㎕
+
| pKD13 template||100 ng/㎕||1㎕
|-
|-
| forward primer||10 pmol||2㎕
| forward primer||10 pmol||2㎕
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*Treatment of PCR products
*Treatment of PCR products
# Add 1㎕ of DpnⅠ to not purified PCR products.
# Add 1㎕ of DpnⅠ to not purified PCR products.
-
# Incubate st 37℃ about 2 hours.
+
# Incubate at 37℃ about 2 hours.
# These samples were purified in elution buffer.
# These samples were purified in elution buffer.
   
   
Line 71: Line 71:
# Wash with ice-cold 10% glycerol 3 times.
# Wash with ice-cold 10% glycerol 3 times.
# Concetrate 100-fold.
# Concetrate 100-fold.
 +
#*Efficiency is
*'''Electroporation'''
*'''Electroporation'''
Line 78: Line 79:
# Incubate 2 hour at 37℃.
# Incubate 2 hour at 37℃.
# Spread one-tenth of the sample and incubate at 37℃.
# Spread one-tenth of the sample and incubate at 37℃.
-
#* 25㎕/ml kanamycin
+
#* Inoculate it to LB broth with 25㎍/ml kanamycin.
*'''
*'''

Revision as of 01:37, 22 October 2010

Contents

Gene replacement

Materials

Procedure

  1. Grow up pKD46, pKD13, and pCP20 in proper host strains
  2. Perform minipreps to extract plasmids
Contents Conc. Vol.
pKD13 template100 ng/㎕1㎕
forward primer10 pmol2㎕
reverse primer10 pmol2㎕
10x EX buffer 5㎕
dNTP2 mM2㎕
EX-tag polymerase 0.5㎕
D.W. 37.5㎕
Total 50㎕
  1. Add 1㎕ of DpnⅠ to not purified PCR products.
  2. Incubate at 37℃ about 2 hours.
  3. These samples were purified in elution buffer.
  1. Pick the single colony containg pKD46.
  2. Inoculate it to 5㎖ LB broth with ampicilline and L-arabinose.
    • L-arabinose final concentration is 1mM.
  3. Incubate at 27℃, 1800rpm until the culture OD reaches 0.6.
  4. Centrifuge 3600rpm, for 5min at 4℃.
  5. Wash with ice-cold 10% glycerol 3 times.
  6. Concetrate 100-fold.
    • Efficiency is
  1. Use 30㎕ competent cell and 300ng PCR product.
  2. Pulse 2.5kV, 200Ω, 25㎌.
  3. Add prewarmed 1㎖ LB broth immediately.
  4. Incubate 2 hour at 37℃.
  5. Spread one-tenth of the sample and incubate at 37℃.
    • Inoculate it to LB broth with 25㎍/ml kanamycin.
  1. Pick the single colony

Notes

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