Team:Stockholm/2 August 2010

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Andreas

CPP DNA synthesis

Designed a CPP cluster to be sent for synthesis, containing all CPPs (with Freiburg prefixes and suffixes) as follows:

(ApaI)—C-Tra10—(BamHI)—N-Tra10—(ClaI)—C-TAT—(NcoI)—N-TAT—(SmaI)—C-LMWP—(BglII)—N-LMWP—(HindIII)

>CPP_cluster
GGGCCCGCGAATTCGCGGCCGCTTCTAGATGGCCGGCGCGGGTTACCTGCTGGGTAAAAT
CAACCTGAAAGCGCTGGCGGCGCTGGCGAAAAAAATCCTGACCGGTTAATACTAGTAGCG
GCCGCTGCAGGCGGATCCGCGAATTCGCGGCCGCTTCTAGATGGCGGGTTACCTGCTGGG
TAAAATCAACCTGAAAGCGCTGGCGGCGCTGGCGAAAAAAATCCTGACCGGTTAATACTA
GTAGCGGCCGCTGCAGGCATCGATGCGAATTCGCGGCCGCTTCTAGATGGCCGGCTACGG
TCGTAAAAAACGTCGTCAGCGTCGTCGTACCGGTTAATACTAGTAGCGGCCGCTGCAGGC
CCATGGGCGAATTCGCGGCCGCTTCTAGATGTACGGTCGTAAAAAACGTCGTCAGCGTCG
TCGTACCGGTTAATACTAGTAGCGGCCGCTGCAGGCCCCGGGGCGAATTCGCGGCCGCTT
CTAGATGGCCGGCGTTTCTCGTCGTCGTCGTCGTCGTGGTGGTCGTCGTCGTCGTACCGG
TTAATACTAGTAGCGGCCGCTGCAGGCAGATCTGCGAATTCGCGGCCGCTTCTAGATGGT
TTCTCGTCGTCGTCGTCGTCGTGGTGGTCGTCGTCGTCGTACCGGTTAATACTAGTAGCG
GCCGCTGCAGGCAAGCTT

Cm stocks

Prepared 4 x 1 ml 25 μg/μl Cm stocks.

LB agar plates

Prepared Cm and Amp LB agar plates as follows:

20x 25 μg/ml Cm
20x 100 μg/ml Amp

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Mimmi

MITF - amplifying and moving the gene to pSB1C3

Using AmplifX, suggested T_a1 = 54.8°C, T_a2 = 62.6°C

Primers

(MW/10)/(OD*33)=df

1000/df=V for 100µM

1:10=V for 10µM

MITF_F: 70.59µl H₂O --> 1:10
MITF_R: 541.88µl H₂O --> 1:10

Mix	(µl)	X4 (µl)	Mix control	(µl)	X5 (µl)	contitions
H₂O	39.5	158	H₂O	22.5	112.5	time	°C
F primer	0.75	3	F primer	1	5	2m	94
R primer	0.75	3	R primer	1	5	30s	94	)
buffer	5	20	DNA	0.5	5*0.5	30s	55	> 5 cycles
Pfx pol	0.5	2	tot	25	125	1m30s	68	)
dNTPs	1.5	6				30s	94	)
MgSO₄	1	4				30s	62	> 25 cycles
DNA	1	4				1m30s	68	)
tot	50	200				10m	68
						oo	10

Nina

PCR on Tyrosinase

I ran a new PCR on the Tyrosinase since I realized that the band from the last PCR on this gene was incorrect (too high than expected). The gene Tyrosinase is about 1900 nt.

PCR Mix (100 ul):

Fprimer 50 uM 1 ul
Rprimer 50 uM 1 ul
dNTP 10 mM 2 ul
Buffer 5X 20 ul for phusion polymerase
Buffer 10X 10 ul for fermenta (Pfu) polymerase
phusion polymerase 1 ul
fermenta (Pfu) polymerase 1 ul
H2O 75 ul for phusion polymerase
H2O 85 ul for fermenta (Pfu) polymerase
DNA template 1 colony

Primer dilutions:

100 uM gets a 1:2 dilution to become 50 uM

cV = cV

100V = 50*10ul

V = 500 / 100 = 5 ul primer and fill up to 10 ul with H2O.

I aliquate the 100 ul in four PCR tubes, each with 25 ul PCR mix.

PCR prgm:

98 °C 2 min

2 * 29 cycles of:

98 °C 30 sec
50-72 °C 30 sec
72 °C 2 min

72 °C 1 min

4 °C ∞

Agarose gel on Tyrosinase

I ran a 1 % agarose gel on the tyrosinase PCR productes.

Ladder: FastRuler™ Middle Range DNA Ladder, ready-to-use, 100-5000 bp Fermentas

Arrangement on gels:

1 = 50 °C - 4 = 72 °C

P1 and 2 look like they have succesfully PCR:ed tyrosinase.

Sequencing yCCS

I send two samples of yCCS for sequencing.

15 ul vector
1.5 ul 10uM VF2 primer

A: ASB0045 246

B: ASB0045 245

The Faculty of Science at Stockholm University

Swedish Vitiligo association (Svenska Vitiligoförbundet)

Revision as of 23:25, 15 August 2010 (view source) NinaSchiller (Talk \| contribs) (→Mimmi) ← Older edit		Latest revision as of 10:45, 26 October 2010 (view source) Hassanforoughiasl (Talk \| contribs)
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