Latest revision as of 14:37, 26 October 2010

Transformation of E. coli

Thaw a 200 µl aliquot of E. coli DH4α and add the transforming DNA (10 ng of vector DNA in 10 µl).
Incubate on ice for 30 minutes.
Heat-shock the cells for 120 seconds at 42°C, and place on ice again for 3-4 minutes.
Add 1 ml of LB broth and incubate the cells at 37°C for 1-1.5 hr in a water bath with gentle shaking.
Plate 200 µl of transformed E. coli onto 1.5% agar plate containing the appropriate selection markers.
Incubate the plates overnight at 37°C.

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-===Protocol===
+{{Team:Newcastle/mainbanner}}
-# Thaw a 200µl aliquot of the desired strain of ''E. coli'' and add the transforming DNA (10 ng of vector DNA in 10 µl). Incubate for 45 min at 42°C.
-# Heat-shock the cells for 120 secs, and place on ice again for 3-4 min.
+=Transformation of ''E. coli''=
-# Add 1ml of LB broth and incubate the cells at 37°C for 1-15 hr in a water bath with gentle shaking.
-# Plate out 100-200 µl/plate on LB (agar at 1.5%), containing the appropriate selection markers.
+==Materials required==
-# Incubate plates overnight at 37°C.
+* ''E. coli'' DH5α (200 µl)
+* Appropriate vector DNA
+* Heat block
+* Bucket of ice
+* Pipettes
+* Eppendorf tubes
+* 1.5% agar plate containing appropriate antibiotics
+==Protocol==
+# Thaw a 200 µl aliquot of ''E. coli'' DH4α and add the transforming DNA (10 ng of vector DNA in 10 µl).
+# Incubate on ice for 30 minutes.
+# Heat-shock the cells for 120 seconds at 42°C, and place on ice again for 3-4 minutes.
+# Add 1 ml of LB broth and incubate the cells at 37°C for 1-1.5 hr in a water bath with gentle shaking.
+# Plate 200 µl of transformed ''E. coli'' onto 1.5% agar plate containing the appropriate selection markers.
+# Incubate the plates overnight at 37°C.
+'''Go back to our [[Team:Newcastle/Protocol list|Protocol List]]'''
+{{Team:Newcastle/footer}}