Bioanalyzer

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(Protocol for Bioanalyzer RNA nano chip)
(Protocol for Bioanalyzer RNA nano chip)
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* vortex dye 10s and spin down
* vortex dye 10s and spin down
* mix one tube gel aliquot with 1µl of dye
* mix one tube gel aliquot with 1µl of dye
-
* vortex, centrifuge 13000g +-20% for 10min
+
* vortex, centrifuge 13000g +-20% for 10min (12000 rpm on Biofuge pico)
* wash electrodes 1min RNase ZAP, 3min water (pipette into 1 well, will spread)
* wash electrodes 1min RNase ZAP, 3min water (pipette into 1 well, will spread)

Revision as of 05:41, 10 March 2011

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The Bioanalyzer is a chip-based capillary electrophoresis machine to analyse RNA, DNA, and protein. It is produced by Agilent and widely used, among other things, in RNA quality control measurements before downstream experiments like microarrays.

Contents

Protocol for Bioanalyzer RNA nano chip

preparation of material

  • prepare max. 12 samples per chip
  • for nano chip max 500ng/µl is recommended, 1000ng/µl is ok
  • denature RNA 70°C 2min, cool on ice

cleaning, gel preparation (start 40min before experiement)

  • take out filtered gel aliquot and fluorescent dye from fridge next door 30min ahead of time (1 gel aliquot tube enough for 2 chips)
  • take out ladder from -80 freezer nextdoor (r145), column 5, nano white box / pico yellow
  • vortex dye 10s and spin down
  • mix one tube gel aliquot with 1µl of dye
  • vortex, centrifuge 13000g +-20% for 10min (12000 rpm on Biofuge pico)
  • wash electrodes 1min RNase ZAP, 3min water (pipette into 1 well, will spread)

prepare chip for measurement

  • take out new RNA chip (pico or nano) from drawer below microarray machine and put into station
  • fill 9µl gel into dark circle G well (gel reservoir)
  • press down plunger and wait 30sec (gel moves through channels)
  • after 30sec release silver trigger (should jump up well above 0.3, meaning seal was tight)
  • wait 5sec, pull plunger up all the way
  • open priming station, add 9µl gel to light circle G wells
  • 5µl of marker into all sample wells and ladder well, bottom right (contains small marker to align plots)
  • 1µl of sample per well, add 1µl of water or replicates into free wells (6µl required per well for machine to run properly)
  • 1µl of ladder into ladder well
  • vortex in holder for 1min and put into machine

start the run

  • start 2100 expert software
  • choose programme for kit: DNA/RNA pico/RNA nano and material: total RNA/mRNA, prokaryotic/eukaryotic
  • start run

wash, export data

  • typical RNA nano run takes just over 20min
  • wash with clean water for 3min immediately after the run has ended (electrodes in the lid will quickly deteriorate otherwise)
  • to export data as PDF you have to print; (PDF option checked will save file, PDF unchecked will print on paper)

expected results

  • expect quantitative range 25–500 ng/μl [claim from the manual]
  • expect quantitation accuracy 20%CV (for ladder as sample) (CV = coefficient of variance) [claim from the manual]

Protocol for Bioanalyzer RNA pico chip

The protocol is very similar for the PICO kit. Similar but reagents adjusted for this kit are used, i.e. a different ladder, marker, and gel.

  • quantitative range 50–5000 pg/μl total RNA, 250-5000 pg/µl mRNA
  • quantitation accuracy 30%CV (for ladder as sample)
  • recommended buffer 50 mM Tris or 50 mM NaCl (assay sensitive to high salt)

Unlike in the nano kit the conditional buffer well has to be filled when using the pico kit.

Troubleshooting

A few typical problems occur once in a while:

  • small RNA marker is not properly (often the next peak is selected => fragments size mislabelled)
cleak peak table, a tab at the bottom of the window; lower marker can be manually set here
  • 18S, 28S not properly assigned (=> RIN number incorrect)

Comments

  • An obscure "serial port" communication errors occurs frequently but can be ignored and has not impact on the readings.

See also

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