Team:Fatih Turkey/ecolitransformation

From 2011.igem.org

(Difference between revisions)
Line 581: Line 581:
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<p><span class="style2">E.coli TOP10 Transformation </span>                                      </p>
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<b><span class="style2">E.coli TOP10 Transformation </span>                                      </b>
<p>MATERIALS </p>
<p>MATERIALS </p>
<p>·         Heat block</p>
<p>·         Heat block</p>
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<p>- Autoclave the bottle.</p>
<p>- Autoclave the bottle.</p>
<p>- After cooling, add 200 uL antibiotic (The LB agar solution should be cool enough not to damage to antibiotic)</p>
<p>- After cooling, add 200 uL antibiotic (The LB agar solution should be cool enough not to damage to antibiotic)</p>
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<p><span class="style5"> Transformation</span></p>
+
<b><span class="style5"> Transformation</span></b>
<p>- Aseptic conditions prepared (70% EtOH, Bunsen burner etc.) </p>
<p>- Aseptic conditions prepared (70% EtOH, Bunsen burner etc.) </p>
<p>- Place 500 uL LB in epp into heat block(42˚C).</p>
<p>- Place 500 uL LB in epp into heat block(42˚C).</p>

Revision as of 17:36, 27 October 2011

deneme baslik

E.coli TOP10 Transformation                                       

MATERIALS

·         Heat block

·         Incubator with shaker

·         Competent cell

·         Lb broth

·         Lb agar with antibiotic

·         Parafilm

·         Sterile MiliQ dH2O

·         Ice

·         0,5 and 1,5 epp

·         Spreader

 

SOLUTIONS

LB Agar Preparation

- Add 200 mL of dH2O to a graduated cyclindar.

- Transfer dH2O into glass bottle.

- Add 7 gr of LB-agar powder

- Autoclave the bottle.

- After cooling, add 200 uL antibiotic (The LB agar solution should be cool enough not to damage to antibiotic)

- Pour the plates .

LB Broth Preparation

- Add 200 mL of dH2O to a graduated cyclindar.

- Transfer dH2O into glass bottle.

- Add 4 gr of LB powder

- Autoclave the bottle.

- After cooling, add 200 uL antibiotic (The LB agar solution should be cool enough not to damage to antibiotic)

 Transformation

- Aseptic conditions prepared (70% EtOH, Bunsen burner etc.)

- Place 500 uL LB in epp into heat block(42˚C).

Thaw 50 uL competent cells on ice.

Add 1 uL plasmid into the competent cell epp and spin for few sec.

Incubate for 45 min on ice.

Incubate at 42˚C for 80 sec in heat block.  

 - Incubate for 5 min on ice.

- Complete to 500 uL with pre-heated LB (42˚C).

-.Epp s adhered with tape to horizontal on shaker.

Incubate at 37 C for 1 h at 240 rpm.

Spread 125 uL from each tube on agar plates with suitable antibiotic.

Incubate plates at 37˚C not longer than 12-14 h.