Team:Heidelberg/Notebook/miMeasure

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(→Seeding and transfection of cells for TECAN, flow cytometry, plate reader and microscopy)
(→Seeding and transfection of cells for TECAN, flow cytometry, plate reader and microscopy)
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5000 Hela and HEK293T cells were seeded on day one in each well of the 96 well plate. Transfection of the constructs (M12-M22) with four different conditions were carried out on day two. The ratio of transfection is 1 (M construct) : 5 (stuffer/ miRsAg/ pcDNA5/ shRNA3) with a total amount of 50ng DNA.
5000 Hela and HEK293T cells were seeded on day one in each well of the 96 well plate. Transfection of the constructs (M12-M22) with four different conditions were carried out on day two. The ratio of transfection is 1 (M construct) : 5 (stuffer/ miRsAg/ pcDNA5/ shRNA3) with a total amount of 50ng DNA.
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Condition a: cotransfected with stuffer (salmon sperm DNA)  
+
Condition a: cotransfection with stuffer (salmon sperm DNA)  
-
Condition b: costransfected with synthetic RNA miRsAg  
+
Condition b: costransfection with synthetic RNA miRsAg  
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Condition c: cotransfected with empty pcDNA5
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Condition c: cotransfection with empty pcDNA5
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Condition d: cotransfected with synthetic shRNA3
+
Condition d: cotransfection with synthetic shRNA3
A control consisting of the empty miMeasure plasmid (without binding site) was also cotransfected wit the same conditions a, b, c and d.
A control consisting of the empty miMeasure plasmid (without binding site) was also cotransfected wit the same conditions a, b, c and d.

Revision as of 19:03, 24 October 2010

miMeasure

Seeding and transfection of cells for TECAN, flow cytometry, plate reader and microscopy

5000 Hela and HEK293T cells were seeded on day one in each well of the 96 well plate. Transfection of the constructs (M12-M22) with four different conditions were carried out on day two. The ratio of transfection is 1 (M construct) : 5 (stuffer/ miRsAg/ pcDNA5/ shRNA3) with a total amount of 50ng DNA.

Condition a: cotransfection with stuffer (salmon sperm DNA)

Condition b: costransfection with synthetic RNA miRsAg

Condition c: cotransfection with empty pcDNA5

Condition d: cotransfection with synthetic shRNA3

A control consisting of the empty miMeasure plasmid (without binding site) was also cotransfected wit the same conditions a, b, c and d.

The cells were used for measurements on day three.

TECAN measurement

The

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