User:Samiye Yaman/Notebook/Lab 571/2011/09/21: Difference between revisions

From OpenWetWare
< User:Samiye Yaman‎ | Notebook‎ | Lab 571‎ | 2011‎ | 09
Jump to navigationJump to search
(Autocreate 2011/09/21 Entry for User:Samiye_Yaman/Notebook/Lab_571)
 
Line 13: Line 13:


==Description==
==Description==
Procedures from the day before was continued
1)A culture media of E.Coli was prepared for the protein expression.
2)GFP containing a cysteine was prepared by using PCR.
-The solution with the wax was was removed from thermocycler.
-By using pipette, the wax was removed from the solution.
-By suing 0.25g of agarose and 25 mL of TAE buffer, 0.01g/mL agarose gel was prepared. There were particles floating in the solution
-The agarose gel was placed into the microwave for 40 seconds in order to have a homogeneous solution.
-The clear homogeneous solution was placed into a mold for 15 min to cool down and solidify.
- More TAE buffer was poured to the top of the agarose gel when it became solid.
-1 ul of blue dye and glycerol mixture and 5uL of PCR were mixed well before loading them into the gel.
-80 V was passed through the gel for 40 min.


==Data==
==Data==

Revision as of 11:54, 26 September 2011

Biomaterials Design Lab <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>

Entry title

Objective

Description

Procedures from the day before was continued

1)A culture media of E.Coli was prepared for the protein expression.

2)GFP containing a cysteine was prepared by using PCR.

-The solution with the wax was was removed from thermocycler.

-By using pipette, the wax was removed from the solution.

-By suing 0.25g of agarose and 25 mL of TAE buffer, 0.01g/mL agarose gel was prepared. There were particles floating in the solution

-The agarose gel was placed into the microwave for 40 seconds in order to have a homogeneous solution.

-The clear homogeneous solution was placed into a mold for 15 min to cool down and solidify.

- More TAE buffer was poured to the top of the agarose gel when it became solid.

-1 ul of blue dye and glycerol mixture and 5uL of PCR were mixed well before loading them into the gel.

-80 V was passed through the gel for 40 min.

Data

  • Add data and results here...

Notes

This area is for any observations or conclusions that you would like to note.


Use categories like tags. Change the "Course" category to the one corresponding to your course. The "Miscellaneous" tag can be used for particular experiments, as instructed by your professor. Please be sure to change or delete this tag as required so that the categories remain well organized.