Berk2010-Christoph: Difference between revisions

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*Colony PCR pMLL6+Bjh2245 in Jtk049. These are not methylated correctly.
*Colony PCR pMLL6+Bjh2245 in Jtk049. These are not methylated correctly.


==[[User:Christoph Neyer|Christoph Neyer]] 19:51, 8 June 2010 (EDT)==
*Ran gel of colony PCR pMLL4-Bjh1882 and pMll5-Bca1091 AGAIN:
[[Image:Colony PCR 2245+1091 Second try.JPG|300px]]
{| {{table}}
| align="center" style="background:#f0f0f0;"|'''ladder'''
| align="center" style="background:#f0f0f0;"|'''1882a'''
| align="center" style="background:#f0f0f0;"|'''b'''
| align="center" style="background:#f0f0f0;"|'''c'''
| align="center" style="background:#f0f0f0;"|'''d'''
| align="center" style="background:#f0f0f0;"|'''1901a(1)'''
| align="center" style="background:#f0f0f0;"|'''b'''
| align="center" style="background:#f0f0f0;"|'''c'''
| align="center" style="background:#f0f0f0;"|'''d'''
| align="center" style="background:#f0f0f0;"|'''ladder'''
| align="center" style="background:#f0f0f0;"|'''1901a(2)'''
| align="center" style="background:#f0f0f0;"|'''b'''
| align="center" style="background:#f0f0f0;"|'''c'''
| align="center" style="background:#f0f0f0;"|'''d'''
|-
|
|}
==[[User:Christoph Neyer|Christoph Neyer]] 16:59, 8 June 2010 (EDT)==
==[[User:Christoph Neyer|Christoph Neyer]] 16:59, 8 June 2010 (EDT)==
*Ligated pMLL6 Eco/Bam digest with part Bjh2245.
*Ligated pMLL6 Eco/Bam digest with part Bjh2245.
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|}
|}
*Ran out of "Righty" cells. So we are transforming Jtk049 with our E/B ligation of pMLL6+Bjh2245.
*Ran out of "Righty" cells. So we are transforming Jtk049 with our E/B ligation of pMLL6+Bjh2245.
==[[User:Christoph Neyer|Christoph Neyer]] 14:04, 8 June 2010 (EDT)==
==[[User:Christoph Neyer|Christoph Neyer]] 14:04, 8 June 2010 (EDT)==
*Digested pMLL6 w/ Eco/Bam and gel purified.
*Digested pMLL6 w/ Eco/Bam and gel purified.

Revision as of 16:51, 8 June 2010



Christoph Neyer 19:37, 8 June 2010 (EDT)

TO DO Tomorrow:

  • Miniprep colonies that we pick for pMLL4+Bjh1882 and pMLL5+Bca1091. These are methylated correctly for the robot.
  • Colony PCR pMLL6+Bjh2245 in Jtk049. These are not methylated correctly.

Christoph Neyer 19:51, 8 June 2010 (EDT)

  • Ran gel of colony PCR pMLL4-Bjh1882 and pMll5-Bca1091 AGAIN:

ladder 1882a b c d 1901a(1) b c d ladder 1901a(2) b c d

Christoph Neyer 16:59, 8 June 2010 (EDT)

  • Ligated pMLL6 Eco/Bam digest with part Bjh2245.
  • Ran gel of colony PCR pMLL4-Bjh1882 and pMll5-Bca1091:

ladder 1882a b c d 1901a(1) b c d ladder 1901a(2) b c d
  • Repicking colonies since Colony PCR appeared contaminated. Block has same layout, shown below:
PCR Block 1882 and 1091 #2 ' ' ' '
1882 1091 #1 1091 #2
A A A
B B B
C C C
D D D
  • Ran out of "Righty" cells. So we are transforming Jtk049 with our E/B ligation of pMLL6+Bjh2245.

Christoph Neyer 14:04, 8 June 2010 (EDT)

  • Digested pMLL6 w/ Eco/Bam and gel purified.
  • Colony PCR of transformed pMLL4-Bjh1882 and pMLL5-Bca1091:
PCR Block 1882 and 1091 #1 ' ' ' '
1882 1091 #1 1091 #2
A A A
B B B
C C C
D D D

Christoph Neyer 19:30, 7 June 2010 (EDT)

Bjh1882 Vectors: AC
Bjh2245 Vectors: KA
Bca1091 Vectors: CK
pMLL4-AC
pMLL5-CK
pMLL6-KA
pMLL7-AK
pMLL8-KC
pMLL9-CA
Bjh1882+pMLL4-AC = Lefty
Bjh2245+pMLL6-KA = Righty
Bca1091+pMLL5-CK = Lefty
Ligated isolated Bjh1882 and Bca1091 into above vectors. Transformed into Lefty strains.
Need to ligate Bjh2245 (Missing pMLL6, need to digest).
TO DO:

  • Digest pMLL6 with Eco/Bam and gel purify. Then ligate with Bjh2245.
  • Check transformed Bjh1882 and Bca1091.
  • Transform ligated Bjh2245+pMLL6 into Righty strain

Christoph Neyer 16:35, 7 June 2010 (EDT)

Couldn't see fragments. Turns out Bjh2245 is 97bp and Bjh1882 is ~680bps.
Re-cut Bjh2245 and Bjh1882.
Small fragment zymo cleanup of Bjh2245 digest.


Gel purified Bjh1882.

Christoph Neyer 15:54, 7 June 2010 (EDT)

Eco/Bam digest of parts: Bjh2245 (LifeACT), Bjh1882 (RFP), and BCA1091 (Ptet).
Gel purified Bjh1882 and Bjh2245.
Small fragment zymo cleanup of BCA1091.