User:Karmella Haynes/Notebook/PcTF Genomics/2013/06/19

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(Autocreate 2013/06/19 Entry for User:Karmella_Haynes/Notebook/PcTF_Genomics)
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'''Line item 1'''<br>
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'''Luciferase activity assay - time point 2'''<br>
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> Samples
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<u>Cell prep</u>
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* Harvested cells
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** Seeded new dox+ plate with 1/2 of cells
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** Pelleted other half, resuspended in 2 mL FACS buffer
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<u>Assay reagents</u>
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* Used the Biotium Steady-Luc Firefly HTS Assay Kit (same as 6/18/13)
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<u>Luc assay</u>
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* Filtered '''700 μL cells''' through strainer caps
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* Other steps same as 6/18/13
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<u>Cell counts</u>
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* Wang lab's Accuri flow cytometer.
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* Set machine to read 20 uL of cells
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* Be sure to "clean" with water-run in between samples
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{| class="wikitable" border="0" cellspacing="3" <!-- Rxn. table -->
{| class="wikitable" border="0" cellspacing="3" <!-- Rxn. table -->
|-valign="top"
|-valign="top"
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| <u>Reagent</u> || <u>Volume</u>  
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| <u>Sample ID</u> || <u>Gated count/ 20 μL</u> || &nbsp; || <u>Cells/ 100 μL</u>
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|-
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| reagent 1 || # μL
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| sample 1 || || x5 = ||
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|-
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| reagent 2 || #
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| sample 2 || || x5 = ||
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|-
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| reagent 3 || #
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| sample 3 || || x5 = ||
|-
|-
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| reagent 4 || #
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| sample 4 || || x5 = ||
|-
|-
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| dH<sub>2</sub>O || #
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| sample 5 || || x5 = ||  
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|-
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| &nbsp; || # μL
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| sample 6 || || x5 = ||  
|}
|}
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--> Reaction conditions
 

Revision as of 00:37, 20 June 2013

Pc-TF Genomics Main project page
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mm/dd/yy

  • Line item 1

Luciferase activity assay - time point 2


Cell prep

  • Harvested cells
    • Seeded new dox+ plate with 1/2 of cells
    • Pelleted other half, resuspended in 2 mL FACS buffer


Assay reagents

  • Used the Biotium Steady-Luc Firefly HTS Assay Kit (same as 6/18/13)


Luc assay

  • Filtered 700 μL cells through strainer caps
  • Other steps same as 6/18/13


Cell counts

  • Wang lab's Accuri flow cytometer.
  • Set machine to read 20 uL of cells
  • Be sure to "clean" with water-run in between samples


Sample ID Gated count/ 20 μL   Cells/ 100 μL
sample 1 x5 =
sample 2 x5 =
sample 3 x5 =
sample 4 x5 =
sample 5 x5 =
sample 6 x5 =



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