"

From 2012.igem.org

Revision as of 19:51, 2 August 2012 (view source) Vadeo (Talk | contribs) ← Older edit		Revision as of 19:52, 2 August 2012 (view source) Vadeo (Talk | contribs) Newer edit →
Line 82:		Line 82:
	<li>Line G & H : LB/MMR medium only (no embryos)		<li>Line G & H : LB/MMR medium only (no embryos)
	</ul>		</ul>
-	<img src="https://static.igem.org/mediawiki/2012/8/8d/SNAP-175407-0003.jpg" alt="result example" />	+	<center><img src="https://static.igem.org/mediawiki/2012/8/8d/SNAP-175407-0003.jpg" alt="result example" /></center>
	</ul>		</ul>
Line 95:		Line 95:
	We put this plate on UV light 15min after the deposit:<br/>		We put this plate on UV light 15min after the deposit:<br/>
-	<img src="https://static.igem.org/mediawiki/2012/a/a9/Wt-0001.jpg" alt="result example"/>	+	<center><img src="https://static.igem.org/mediawiki/2012/a/a9/Wt-0001.jpg" alt="result example"/></center>
	<h2>Thursday, 21st June</h2>		<h2>Thursday, 21st June</h2>

---

Revision as of 19:52, 2 August 2012

Weeks

1

2

3

4

5

6

7

8

9

10

11

12

13

14

15

16

Week 2: 18th June - 24th June

Monday, 18th June

• Inoculation
• Auxin and salkowski's test purchased

Tuesday, 19th June

Miniprep

• J23100 RFP: 101.9 ng/uL
  
• K515100 Auxin: 319.7 ng/uL
  

Misc

Liquid culture of aux and RFP

Wednesday, 20th June

Previous work :

Liquid culture of DH5a with mRFP and auxin plasmid

Main goals:

1. Auxin toxicity test
2. Bacterial integration assessment into the xenopus embryos

Experiments

1. Xenopus embryos present a protective membrane, we decided to realize our bacterial deposits experiments on xenopus with and without their membrane. Then, we could see if bacterias could enter into the embryos naturally.
2. On 96 plates, each plate contains 1 embryo:
   • Plate 1:
     • Line A & B = on embryos without protective membrane : 500 uL mRFP plasmid on DH5a deposite + 1mL LB + 1mL MMR medium
       
     • Line C : 1 2 3 : normal embryos : 500 uL mRFP plasmid on DH5a deposite + 1mL (LB + MMR medium)
       
     • Line E & F = embryos without protective membrane : 500 uL AUX plasmid integrated on DH5a deposit + 1mL LB + 1mL MMR medium
       
     • Line G & M1-6 = normal embryos : 500 uL AUX plasmid integrated on DH5a deposit + 1mL LB + 1mL MMR medium
       
     • Line M7-9 = normal embryos : controls
   • Plate 2 (normal embryos only):
     • Line A & B
     • Line C : LB/MMR medium
     • Line D : RFP 0.1uL
     • Line E : AUX 0.1uL
     • Line G & H : LB/MMR medium only (no embryos)
     
3. On 16 Plates each plate contains 3 tadpoles:
   • Line A : 0.5uL RFP bacteria
   • Line B1 : 0.3uL RFP bacteria
   
   

We put this plate on UV light 15min after the deposit:

Thursday, 21st June

Friday, 22nd June