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Team:Newcastle/15 June 2010
From 2010.igem.org
(Difference between revisions)
| Line 6: | Line 6: | ||
# To clean Nanodrop, add a drop of water on the spectrometer and press blank | # To clean Nanodrop, add a drop of water on the spectrometer and press blank | ||
# After cleaning, wipe the water off | # After cleaning, wipe the water off | ||
| - | # To equalizen the equipment, add | + | # To equalizen the equipment, add 3 μl of the buffer used in the sample and press blank |
# Wipe the buffer off | # Wipe the buffer off | ||
| - | # To measure sample, add | + | # To measure sample, add 3 μl of the sample and press measure |
# If dealing with multiple samples, clean the equipment with water at regular intervals | # If dealing with multiple samples, clean the equipment with water at regular intervals | ||
# After measurement, clean the equipment with a drop of water on the spectrometer and press blank | # After measurement, clean the equipment with a drop of water on the spectrometer and press blank | ||
| Line 16: | Line 16: | ||
Gel electrophoresis can used to separate DNA, RNA, or protein molecules by molecular weight using an electric field applied to a gel matrix | Gel electrophoresis can used to separate DNA, RNA, or protein molecules by molecular weight using an electric field applied to a gel matrix | ||
| - | # Make up 1% agarose gel (1g of agarose in | + | # Make up 1% agarose gel (1g of agarose in 100 ml of TAE buffer) and transfer 60 ml of molten agarose gel into the gel tray with 3 μl of Safeview |
| - | # Wait for | + | # Wait for 30 min to allow the gel to harden |
# Transfer harden gel into the gel tank and add TAE buffer until the gel is completely submerge | # Transfer harden gel into the gel tank and add TAE buffer until the gel is completely submerge | ||
# Depending on the nature of the sample, 3μl of GeneRuler™ 1kb Plus DNA Ladder was used for analysing DNA | # Depending on the nature of the sample, 3μl of GeneRuler™ 1kb Plus DNA Ladder was used for analysing DNA | ||
# Loading buffer was then added together with the sample before loading onto the gel matrix | # Loading buffer was then added together with the sample before loading onto the gel matrix | ||
# Run gel at 90V until separation is achieved and visualize using the gelDoc | # Run gel at 90V until separation is achieved and visualize using the gelDoc | ||
Revision as of 09:54, 17 June 2010
Nanodrop protocol
Nanodrop can be used to measure the DNA, RNA and protein
- Select Nanodrop program from the desktop
- To clean Nanodrop, add a drop of water on the spectrometer and press blank
- After cleaning, wipe the water off
- To equalizen the equipment, add 3 μl of the buffer used in the sample and press blank
- Wipe the buffer off
- To measure sample, add 3 μl of the sample and press measure
- If dealing with multiple samples, clean the equipment with water at regular intervals
- After measurement, clean the equipment with a drop of water on the spectrometer and press blank
Gel electrophoresis
Gel electrophoresis can used to separate DNA, RNA, or protein molecules by molecular weight using an electric field applied to a gel matrix
- Make up 1% agarose gel (1g of agarose in 100 ml of TAE buffer) and transfer 60 ml of molten agarose gel into the gel tray with 3 μl of Safeview
- Wait for 30 min to allow the gel to harden
- Transfer harden gel into the gel tank and add TAE buffer until the gel is completely submerge
- Depending on the nature of the sample, 3μl of GeneRuler™ 1kb Plus DNA Ladder was used for analysing DNA
- Loading buffer was then added together with the sample before loading onto the gel matrix
- Run gel at 90V until separation is achieved and visualize using the gelDoc
