Team:TU Darmstadt/Protocols/DNA Quantification / NanoDrop

From 2012.igem.org

(Difference between revisions)
(Created page with "<html> <link rel="stylesheet" href="https://2012.igem.org/wiki/index.php?title=Team:TU_Darmstadt/css&action=raw&ctype=text/css" type="text/css" /> <div id="TUD"> <div id="...")
Line 46: Line 46:
DNA absorbs light at 260 nm and thus the concentration can be measured photometrically using the [http://www.nanodrop.com/Library/nd-1000-v3.7-users-manual-8.5x11.pdf NanoDrop 1000 Spectrophotometer].
DNA absorbs light at 260 nm and thus the concentration can be measured photometrically using the [http://www.nanodrop.com/Library/nd-1000-v3.7-users-manual-8.5x11.pdf NanoDrop 1000 Spectrophotometer].
-
==== Measuring ====
+
==== NanoDrop 1000 ====
-
#Start the programme for the NanoDrop 1000 and click “Nucleic Acids”
+
#Start the programme for the NanoDrop 1000 and click '''Nucleic Acids'''
#Pipette 1.5 µL of a water sample onto the lower measurement and click “OK”
#Pipette 1.5 µL of a water sample onto the lower measurement and click “OK”
#Load your blank and click '''Blank'''
#Load your blank and click '''Blank'''
Line 53: Line 53:
#At the end load your blank and click '''Measure''' to test the blank.
#At the end load your blank and click '''Measure''' to test the blank.
#If the measurement deviates more than 5 ng/µL from 0.0 ng/µL, load the blank again, click '''Blank''' and measure your DNA samples.
#If the measurement deviates more than 5 ng/µL from 0.0 ng/µL, load the blank again, click '''Blank''' and measure your DNA samples.
 +
==== Shimandzu NanoDrop ====
 +
Switch the NanoDrop ON make sure a wiper is attatched.
 +
# Press F3 to blank with 2µl of dH<sub>2</sub>O eg.
 +
# Put 1-2µl of solution of the NanoDrop lense
 +
# Press F4 to measure

Revision as of 00:16, 12 September 2012

Contents

DNA Quantification

Visual Comparison

It is possible to determine DNA concentrations by comparing the relative intensity of PCR bands and marker in agarose gel.

Nanodrop

DNA absorbs light at 260 nm and thus the concentration can be measured photometrically using the [http://www.nanodrop.com/Library/nd-1000-v3.7-users-manual-8.5x11.pdf NanoDrop 1000 Spectrophotometer].

NanoDrop 1000

  1. Start the programme for the NanoDrop 1000 and click Nucleic Acids
  2. Pipette 1.5 µL of a water sample onto the lower measurement and click “OK”
  3. Load your blank and click Blank
  4. Load your DNA samples and click Measure. A 260/280 ration of 1.8 or above means the sample can be seen as pure
  5. At the end load your blank and click Measure to test the blank.
  6. If the measurement deviates more than 5 ng/µL from 0.0 ng/µL, load the blank again, click Blank and measure your DNA samples.

Shimandzu NanoDrop

Switch the NanoDrop ON make sure a wiper is attatched.

  1. Press F3 to blank with 2µl of dH2O eg.
  2. Put 1-2µl of solution of the NanoDrop lense
  3. Press F4 to measure