User:Karmella Haynes/Notebook/BioBrick cloning/2015/06/23: Difference between revisions
From OpenWetWare
(fix raw html notebook nav) |
|||
(6 intermediate revisions by one other user not shown) | |||
Line 2: | Line 2: | ||
|- | |- | ||
|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;">Karmella's BioBrick Cloning</span> | |style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;">Karmella's BioBrick Cloning</span> | ||
|style="background-color: #F2F2F2" align="center"| | |style="background-color: #F2F2F2" align="center"|[[File:Report.png|frameless|link={{#sub:{{FULLPAGENAME}}|0|-11}}]][[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|[[File:Resultset_previous.png|frameless|link={{#lnpreventry:{{FULLPAGENAME}}}}]][[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]] }}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]][[File:Resultset_next.png|frameless|link={{#lnnextentry:{{FULLPAGENAME}}}}]]}} | ||
|- | |- | ||
| colspan="2"| | | colspan="2"| | ||
Line 29: | Line 29: | ||
| bgcolor=#cfcfcf | Reagent | | bgcolor=#cfcfcf | Reagent | ||
| bgcolor=#cfcfcf | Volume | | bgcolor=#cfcfcf | Volume | ||
| rowspan="7" | [[Image:KAH062315_gel1.jpg| | | rowspan="7" | [[Image:KAH062315_gel1.jpg|150px|Hover name]]<br>30 μL/lane, 1% agarose; [http://openwetware.org/wiki/Image:KAH_Fermentas_GeneRuler_1kbplus.jpg Ladder] | ||
|- | |- | ||
| DNA (plasmid) || 20.0 | | DNA (plasmid) || 20.0 | ||
Line 49: | Line 49: | ||
* DpnI digest & clean-up of PCR products | * DpnI digest & clean-up of PCR products (inserts) | ||
** Add 1 μL DpnI to each PCR rxn. Incubate @ 37°C/ 5 min. | ** Add 1 μL DpnI to each PCR rxn. Incubate @ 37°C/ 5 min. | ||
** Use the Qiagen Qiaquick PCR Purification kit (cat. no. 28104 ) to purify DNA. | ** Use the Qiagen Qiaquick PCR Purification kit (cat. no. 28104 ) to purify DNA. | ||
Line 131: | Line 131: | ||
|} | |} | ||
RESULTS (5/ | RESULTS (6/24/15) | ||
* | * SUCCESS! Plate 6 (neg ctrl) has 7 colonies; Plates 1-5 have 30 - 50 colonies | ||
* Pick two clones from each for 5 mL cultures/ minipreps | |||
---- | |||
'''Rene - CRISPR PCR library PCR''' | |||
* '''Part 1 - GoTaq "Dirty" PCR on liquid mini-cultures, 600 bp amplicons; primers P163/P215''' | |||
* Part 2 - Nested SYBR real time PCR & melt curves on (1) mini cultures, (2) amplicons from GoTaq | |||
* Part 1 - GoTaq "Dirty" PCR on liquid mini-cultures, 600 bp amplicons | |||
** Clone labeling notes, changed from last time: | |||
*** L34 = Luc14 cells treated with gRNA034 | |||
*** G34 = Gal4EED/luc cells treated with gRNA034 | |||
*** 001, 002, 003 = clone no. | |||
*** A01, A02, etc. = well position in dish or spot on agar array | |||
1-96. L34_097_A01 - L34_192_H12 (full plate)<br> | |||
{| {{table}} cellspacing="3" <!-- PCR rxn. table --> | |||
|- valign="top" | |||
| bgcolor=#cfcfcf | Reagent | |||
| bgcolor=#cfcfcf | Rxn1-24 | |||
| bgcolor=#cfcfcf | Mix (x104) | |||
| rowspan="7" | Expected:<br>PCR insert/ pJET = ~600 bp<br>1. L34_097_A01<br>2. L34_109_B01<br>3. L34_121_C01<br>4. L34_133_D01<br>5. L34_145_E01<br>6. L34_157_F01<br>7. L34_169_G01<br>8. L34_181_H01 | |||
| rowspan="7" | Gel showed no signal | |||
|- | |||
| Template (culture) || 2.0 || --- | |||
|- | |||
| 10 uM fwd primer || 1.0 || 104.0 | |||
|- | |||
| 10 uM rev primer || 1.0 || 104.0 | |||
|- | |||
| 2x GoTaq (clear) || 12.5 || 1300.0 | |||
|- | |||
| dH<sub>2</sub>O || 8.5 || 884.0 | |||
|- | |||
| || 25.0 μL | |||
|} | |||
* Note: Master Mix Multiplier (for one 96-well plate) = 96 + 1 extra 8-well column = 104 | |||
* Aliquot 200 μL into 8 tubes in 8-tube strip | |||
* Use multichannel to aliquot 23 μL to 96-well plate, 1 column at a time | |||
* Refill the 8-tube strip as needed with enough to fill remaining columns | |||
PCR - Labnet: "GoTaq35KAH" | |||
* '''98°C, 10 min''' | |||
* 35x[95°C, 10 sec; 60°C, 10 sec; 72°C, 20 sec] | |||
* 72°C, 3 min | |||
* 4°C ∞ | |||
CONCLUSIONS | |||
* Looks like amplification failed | |||
* Move on to sequencing of all clones | |||
* Restart fresh cultures tomorrow | |||
* Will submit as pellets to DNASU | |||
Latest revision as of 01:01, 27 September 2017
Karmella's BioBrick Cloning | Main project page Previous entry Next entry | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
06/23/15
Cas-tone Assemblies
Thermal cycler: LabNet OptiMax "AnOlig shrt"
RESULTS (6/24/15)
Rene - CRISPR PCR library PCR
1-96. L34_097_A01 - L34_192_H12 (full plate)
|