Xenopus gene collection (XGC) plates

 

 

Please note that the plate(s) being sent have tested negative in our phage contamination assay. However these plates should still be handled with care as no phage assay can be guaranteed to be 100%

What to do with your clones when you receive them

 

IRBH (Xenopus laevis) and IRBN (Xenopus tropicalis)

Plates have been replicated in LB broth containing 8% glycerol and 50µg/ml ampicillin.
The plates have been shipped frozen in dry ice and should be placed in a -70°C freezer on arrival.
To make further copies replicate in the above media and incubate overnight at 37°C.

 

IRBG (Xenopus laevis)

Plates have been replicated in LB broth containing 8% glycerol and 27µg/ml chloramphenicol.
The plates have been shipped frozen in dry ice and should be placed in a -70°C freezer on arrival.
To make further copies replicate in the above media and incubate overnight at 30°

 

Vector information

In each of these subsets all clones on one plate share the same vector. For details of vectors used follow these links:

IRBG (Xenopus laevis)

IRBH (Xenopus laevis

IRBN (Xenopus tropicalis)

Vector information can be found here.

 

Recommended methods for isolation and purification of DNA

Plasmid DNA mini-prep preparation

Any standard mini-prep method is suitable. Below is the method used in-house at Source BioScience.


a) Streak out plasmid onto LB + ampicillin (or chloramphenicol [CM]) plate. Incubate overnight at 37°C (amp.) or 30°C (CM).

b) Dispense 5ml LB medium into a 50ml sterile tube. Add appropriate antibiotic. Inoculate with a single colony and incubate overnight in shaking incubator 37°C [30°C (CM)]/170 rpm.

c) [If a glycerol stock is required, transfer aliquot of 140µl to a 1.5ml microtube. Add 40µl 80 % glycerol. Mix and freeze.]

d) Take 2ml of the plasmid broth, transfer to a 2ml microtube, and centrifuge 15 min 3000 rpm.


e) Pour off supernatant and discard. Re-suspend pellet in 200µl GTE. Add 5µl RNAase A stock (10mg/ml). Incubate 10 min. room temperature.

f) Lysis: Add 400µl 0.2M NaOH/1% SDS (freshly made). Mix by inversion. Place on ice for 5 min.


g) Add 300µl 3M K Ac. Invert to mix. Place on ice for 10 min

h) Centrifuge 10 min at 13000 rpm in microfuge. Decant supernatant into a 1.5ml microtube
containing 1ml cold ethanol, vortex briefly and leave to stand for 30 min. on ice.

i) Centrifuge 10 min. at 13000 rpm in microfuge. Remove ethanol carefully (preferably by suction technique).

j) Add 200µl cold 70% ethanol, vortex briefly, centrifuge 10 min. at 13000 rpm in microfuge, remove ethanol carefully (as above).

k) Air dry pellet. Add 50µl TE and leave to re-suspend overnight at 4°C.

 

Solutions:

10 ml GTE:

0.5 ml 20% glucose
0.25 ml 1M Tris/HCl pH 7.5
0.2 ml 0.5M EDTA pH 8.0.
9.05 ml sterile distilled water

Lysis Buffer:

100 ml 0.2M NaOH/1% SDS = 0.8 g NaOH
5ml 20% SDS
95ml sterile distilled water.


PEG purification of plasmid DNA (strongly recommended before sequencing)

 

a) Add an equal volume of 20% PEG solution in 2.5M NaCl. Incubate at room temperature for 5-10 min.
Spin for 10-15 min. at 13,000 rpm.

b)
Remove supernatant and rinse pellet with 70% ethanol. Dry the pellet. Resuspend in 20µl sterile
distilled water.

c)
Remove 5µl and add to 2µl loading buffer. Run out with appropriate DNA marker on a 1.5% TBE
agarose gel to check that DNA recovery is good.

d)
The DNA is now ready for sequencing.

General PCR Purification Method

Clones can be amplified by PCR using the appropriate flanking primers. PCR products should then be purified using spin columns or the sAP/exo1 (shrimp alkaline phosphatase/exonuclease1) method prior to sequencing.

Werle. E, Schneider. C, Renner. M, Volker.M and Fiehn. W. (1994) Convenient single-step, one tube purification of PCR products for direct sequencing. Nucl. Acids Res. 22: 4354-4355.

Hanke. M and Wink. M. (1994) Direct DNA sequencing of PCR-amplified vector inserts following enzymatic degradation of primer and dNTPs. BioTechniques 17: 858-860.