Team:UNIPV-Pavia/Calendar/July/settimana2

July, 4th

Digestions of previously purified plasmids were performed for ligations:

Plasmid	Kind	Purified DNA (μl)	H2O (μl)	Enzyme 1 (μl)	Enzyme 2 (μl)	Buffer H (μl)	Final Volume(μl)
<partinfo>BBa_C0060</partinfo>	Insert	16.5	4	1 EcoRI	1 SpeI	2.5	25
<partinfo>BBa_C0061</partinfo>	Insert	13.2	7.3	1 XbaI	1 PstI	2.5	25
<partinfo>BBa_K081022</partinfo>	Insert	15.7	4.8	1 EcoRI	1 PstI	2.5	25
<partinfo>BBa_B0030</partinfo>	Vector	13.2	7.3	1 SpeI	1 PstI	2.5	25
<partinfo>BBa_B0031</partinfo>	Vector	12.4	8.1	1 SpeI	1 PstI	2.5	25
<partinfo>BBa_B0032</partinfo>	Vector	9.5	11	1 SpeI	1 PstI	2.5	25
<partinfo>BBa_B0015</partinfo>	Vector	7.9	12.6	1 EcoRI	1 XbaI	2.5	25
<partinfo>pSB4C5</partinfo>	Vector	3	17.5	1 EcoRI	1 PstI	2.5	25
<partinfo>BBa_I13501</partinfo>	Insert	7.2	13.3	1 XbaI	1 PstI	2.5	25

Reactions were incubated at 37°C for three hours while a small-size and a medium-size agarose gel were prepared according to protocols.

In the afternoon gel electrophoresis was performed.

[[Image:UNIPV_04_07_MSgel.png|frame|center|300px|Medium size gel]]

As shown, in figure all clones were positive (apart from <partinfo>BBa_I13501</partinfo> run where we inexplicably didn't see any band), so we cut and purified the bands of interest. Cells harbouring <partinfo>BBa_I13501</partinfo> were again inoculated in 5 ml LB + Amp.

After gel extraction, cut DNA was quantified:

Plasmid	Purified DNA ng/μl
<partinfo>BBa_C0060</partinfo> (E-S)	3.9
<partinfo>BBa_C0061</partinfo> (X-P)	4.1
<partinfo>BBa_K081022</partinfo> (E-P)	4.4
<partinfo>BBa_B0030</partinfo> (S-P)	10.3
<partinfo>BBa_B0031</partinfo> (S-P)	11.8
<partinfo>BBa_B0032</partinfo> (S-P)	10.1
<partinfo>BBa_B0015</partinfo> (E-X)	12
<partinfo>pSB4C5</partinfo> (E-P)	10.7

Then ligations were performed in a final volume of 10 μl:

Ligation Name	Vector	Vector μl	Insert	Insert μl	Buffer μl	T4 Ligase μl
E1	<partinfo>BBa_B0015</partinfo> (E-X)	1.5	<partinfo>BBa_C0060</partinfo> (E-S)	6.5	1	1
E2	<partinfo>BBa_B0030</partinfo> (S-P)	1.5	<partinfo>BBa_C0061</partinfo> (X-P)	6.5	1	1
E3	<partinfo>BBa_B0031</partinfo> (S-P)	1.5	<partinfo>BBa_C0061</partinfo> (X-P)	6.5	1	1
E4	<partinfo>BBa_B0032</partinfo> (S-P)	1.5	<partinfo>BBa_C0061</partinfo> (X-P)	6.5	1	1
E8	<partinfo>pSB4C5</partinfo> (E-P)	1.5	<partinfo>BBa_K081022</partinfo> (E-P)	6.5	1	1

Ligations were incubated ON at 16°C.

July, 5th

T4 Ligase was inactivated, heating ligations at 65°C for 10 minutes; ligations were stored at -20°C. Plasmid purification was done again for <partinfo>BBa_I13501</partinfo> and purified DNA was quantified:

Plasmid	Purified DNA ng/μl
<partinfo>BBa_I13501</partinfo>	97.2

<partinfo>BBa_I13501</partinfo> was then digested with restriction endonucleases:

Plasmid	Kind	Purified DNA (μl)	H2O (μl)	Enzyme 1 (μl)	Enzyme 2 (μl)	Buffer H (μl)	Final Volume(μl)
<partinfo>BBa_I13501</partinfo>	Insert	10.5	10	1 XbaI	1 PstI	2.5	25

According to protocols the reaction was incubated at 37°C for 3 hours.
60 ml of 80% glycerol were prepared mixing 48 ml of 100% glycerol with 12 ml of ddH₂O.
Gel electrophoresis was done for <partinfo>BBa_I13501</partinfo> digestion:

Cut DNA was gel-extracted:

Plasmid	Purified DNA ng/μl
<partinfo>BBa_I13501</partinfo> (X-P)	2.6

Further ligations were prepared and incubated ON at 16°C:

Ligation Name	Vector	Vector μl	Insert	Insert μl	Buffer μl	T4 Ligase μl
E5	<partinfo>BBa_B0030</partinfo> (S-P)	1	<partinfo>BBa_I13501</partinfo> (X-P)	7	1	1
E6	<partinfo>BBa_B0031</partinfo> (S-P)	1	<partinfo>BBa_I13501</partinfo> (X-P)	7	1	1
E7	<partinfo>BBa_B0032</partinfo> (S-P)	1	<partinfo>BBa_I13501</partinfo> (X-P)	7	1	1

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