User:Karmella Haynes/Notebook/PcTF Genomics/2013/06/12: Difference between revisions

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==mm/dd/yy==
==06/12/13==
<!-- Precede finished items with a checkmark &#x2713; -->
<!-- Precede finished items with a checkmark &#x2713; -->
* Line item 1
* Gal4-EED/luc cells IFC - stain with anti-luc overnight
* PcTF transfection of U2OS
 
 
----
'''Gal4-EED/luc cells IFC'''<br>
* Samples: first row of wells in the 24-well plate.
* Keep all others under PBS
 
# 0 μg/mL dox
# 0.1  
# 0.2
# 0.5
# 1.0
# 2.0 (induced on 6/02/13, 10 days)
 
* Use 1:200 dilution of rabbit (poly) anti-luc (in 15 μL Gentex horse serum blocking solution per well)
* Incubate under parafilm "covers" overnight at 4°C in box with wet paper towels
 


----
----
'''Line item 1'''<br>
'''Lipo transfection'''<br>
> Samples
> Cells were 100% confluent<br>
> Re-plate 1:2 dilution prior to transfection in 3.4 mL p/s-free medium<br>
> Transfect human PcTF under control of constitutive CMV promoter (KAH160/MV1); 346.6 ng/μL<br>
> Samples are for RT-PCR


{| class="wikitable" border="0" cellspacing="3" <!-- Rxn. table -->
 
|-valign="top"
{| class="wikitable" border="0" cellspacing="5" <!-- Lipofectamine transfection table -->
| <u>Reagent</u> || <u>Volume</u>  
|-
|-
| reagent 1 || # μL
| <u>Wells</u> || <u>Plasmid</u> || <u>DNA</u> || <u>Volume + dH<sub>2</sub>O</u> || <u>Opti-MEM</u> || <u>PLUS</u> || <u>Lipo</u>  ||  
|-
|-
| reagent 2 || #
| 1            || KAH160/MV1        || 2 μg      || 5.8 μL +14.2  || 570 μL          || 2.5 μL          || 7.5 μL
|-
|-
| reagent 3 || #
| 2            || KAH160/MV1        || 2 μg      || 5.8 μL +14.2  || "            || "          || "
|-
|-
| reagent 4 || #
| 3            || KAH160/MV1        || 2 μg    || 5.8 μL +14.2  || "            || "          || "
|-
|-
| dH<sub>2</sub>O || #
| 4            || mock        || none    || 0 μL + 20.0  || "            || "          || "
|-
|-
| &nbsp; || # μL
| 5            || mock        || none    || 0 μL + 20.0  || "            || "          || "
|-
| 6            || mock          || none      || 0 μL + 20.0          || "          || "          || "
|}
|}


--> Reaction conditions
> Add 570 μL Opti-MEM to each 20 μL DNA sample <br>
> Add 2.5 μL PLUS reagent to each DNA+Opti-MEM sample. 5 min/room temp<br>
> Add 7.5 μL Lipofectamine LTX to each DNA+Opti-MEM+PLUS reagent sample. 30 min/ room temp <br>
> Add 600 μL complexes to each well (final volume of medium = 4 ml/well)<br>
> Grow cells at 37&deg;C overnight<br>
 
 
 




Revision as of 14:02, 30 June 2013

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06/12/13

  • Gal4-EED/luc cells IFC - stain with anti-luc overnight
  • PcTF transfection of U2OS


Gal4-EED/luc cells IFC

  • Samples: first row of wells in the 24-well plate.
  • Keep all others under PBS
  1. 0 μg/mL dox
  2. 0.1
  3. 0.2
  4. 0.5
  5. 1.0
  6. 2.0 (induced on 6/02/13, 10 days)
  • Use 1:200 dilution of rabbit (poly) anti-luc (in 15 μL Gentex horse serum blocking solution per well)
  • Incubate under parafilm "covers" overnight at 4°C in box with wet paper towels


Lipo transfection
> Cells were 100% confluent
> Re-plate 1:2 dilution prior to transfection in 3.4 mL p/s-free medium
> Transfect human PcTF under control of constitutive CMV promoter (KAH160/MV1); 346.6 ng/μL
> Samples are for RT-PCR


Wells Plasmid DNA Volume + dH2O Opti-MEM PLUS Lipo
1 KAH160/MV1 2 μg 5.8 μL +14.2 570 μL 2.5 μL 7.5 μL
2 KAH160/MV1 2 μg 5.8 μL +14.2 " " "
3 KAH160/MV1 2 μg 5.8 μL +14.2 " " "
4 mock none 0 μL + 20.0 " " "
5 mock none 0 μL + 20.0 " " "
6 mock none 0 μL + 20.0 " " "

> Add 570 μL Opti-MEM to each 20 μL DNA sample
> Add 2.5 μL PLUS reagent to each DNA+Opti-MEM sample. 5 min/room temp
> Add 7.5 μL Lipofectamine LTX to each DNA+Opti-MEM+PLUS reagent sample. 30 min/ room temp
> Add 600 μL complexes to each well (final volume of medium = 4 ml/well)
> Grow cells at 37°C overnight





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