|
| Status |
Public on Aug 16, 2007 |
| Title |
NZ7603_vs_WCFS1 |
| Sample type |
RNA |
| |
|
| Channel 1 |
| Source name |
mutant trxB2
|
| Organism |
Lactiplantibacillus plantarum |
| Characteristics |
L. plantarum strain NZ7603 trxB2::cam cultivated UNDER RESPIRATORY CONDITIONS (+OXYGEN +HEME +VITAMIN K2)
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Extraction RNA
Collecting cells
Quenching Buffer
66.7 mM HEPES (pH 6.5) 60% Methanol
Extraction Mixture (Prepared in a screw-cap tube)
-500 µll phenol/Chloroform
-30 µl 10% SDS
-30 µl 3 M NaAc (pH 5.2)
-500 mg glass-beads (75-150 µm)
-400 µl TE buffer
1.For each sample prepare a tube with Extraction Mixture
2.Harvest cells and quench them immediately in Quenching Buffer. Add 4 volumes of Quenching Buffer ( 40°C) to 1 volume of cell culture
3.Mix and store the sample at -40°C
4.Centrifuge cells at -20 C at 9000 rpm for 10 minutes (Centrifuge RC5B)
5.Discard the supernatant; keep the cell pellet cooled and work quickly to prevent condensation of water. Transfer the pellet with a pre-cooled spatula to a screw-crap tube with Extraction Mixture
6.Mix the cell pellet thoroughly with Extraction Mixture by shaking by hand
7.Freeze the tube immediately in liquid nitrogen
8.Break cells in the Savant FastPrep FP120. Three times 40 seconds at speed 4.0 (cool cells between steps if necessary)
9.Centrifuge for 5 minutes at 4°C in an Eppendorf centrifuge at 10.000 rpm
10.Transfer 500 µl of the supernatant to a new tube. Add 400 µl chloroform (chloroform should be cooled at 4°C)
11.Centrifuge for 2 minutes in an Eppendorf centrifuge at full speed (4°C)
5.Continue with the "High Pure RNA Isolation Kit" from Roche (order # 1 828 665)
6.Incubate for 60 minutes with DnaseI, elute with 50 µl elution buffer
7.Store the RNA in at least 2 aliquots, one of 20 µl (for concentration and quality analysis and labeling) and one back-up of 30 µl at 80°C.
|
| Label |
Cy3
|
| Label protocol |
cDNA synthesis and Labeling Protocol 1.4
Annealing Annealing Mix
x µl RNA preparation (=10 µg)
y µl nuclease-free water
1 µl Random Nonamers
11 µl TOTAL
1.mix Annealing Mix in a 200 µl PCR tube gently by pipetting up and down
2.incubate for 5’ 70°C
3.cool at room temperature for 10’ (annealing)
4.spin down the mixture to the bottom of the tube
5.place on ice Reverse transcription
Reverse Transcription Mix
4 µl 5x buffer
2 µl 0.1 M DTT
1 µl dNTP-mix
1 µl AA-dUTP
1 µl TMIII (keep only briefly outside 20°C)
20 µl TOTAL
1.Mix by very gently by pipetting up and down.
2.Incubate for 3 hrs at 42°C (in PCR-machine)
3.Cool on ice for immediate purification or place at 20°C for storage
Degradation of mRNA
1.Add 2 µl 2,5 M NaOH
2.Mix (vortex) and spin down
3.Incubate for 15 min. at 37°C
4.Add 10 µl 2 M HEPES free acid
5.Mix (vortex) and spin down
6.Ready for purification or store at 20°C
Labelling of cDNA with cyanine dyes Purification of amino allyl-modified cDNA Followed Ge Healthcare kit "Amersham CyDye (Cy3/Cy5)Reactive Dye Protocols for Post Labelling Aminoallyl-cDNA and Aminoallyl-aRNA" code RPN5661
Labelling of amino allyl-modified cDNA with CyDye
1.Add the amino allyl modified cDNA (in 0.1 M sodium bicarbonate) directly into one aliquot of CyDye NHS Ester. Resuspend the ester completely by pipetting several times and transfer the solution to an amber 1.5 ml tube
2.Incubate at room temperature, in the dark for 60 to 90 minutes
3.Add 15 µl 4 M Hydroxylamine to each coupling reaction
4.Mix by stirring and incubate at room temperature, in the dark, for 15 minutes
5.Proceed directly to purification of CyDye-labelled cDNA following Ge Healthcare kit "Amersham CyDye (Cy3/Cy5)Reactive Dye Protocols for Post Labelling Aminoallyl-cDNA and Aminoallyl-aRNA" product code RPN5661
|
| |
|
| Channel 2 |
| Source name |
WT
|
| Organism |
Lactiplantibacillus plantarum |
| Characteristics |
L. plantarum strain WCFS1 (wild type) cultivated UNDER RESPIRATORY CONDITIONS (+OXYGEN +HEME +VITAMIN K2)
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Extraction RNA
Collecting cells
Quenching Buffer
66.7 mM HEPES (pH 6.5) 60% Methanol
Extraction Mixture (Prepared in a screw-cap tube)
-500 µll phenol/Chloroform
-30 µl 10% SDS
-30 µl 3 M NaAc (pH 5.2)
-500 mg glass-beads (75-150 µm)
-400 µl TE buffer
1.For each sample prepare a tube with Extraction Mixture
2.Harvest cells and quench them immediately in Quenching Buffer. Add 4 volumes of Quenching Buffer ( 40°C) to 1 volume of cell culture
3.Mix and store the sample at -40°C
4.Centrifuge cells at -20 C at 9000 rpm for 10 minutes (Centrifuge RC5B)
5.Discard the supernatant; keep the cell pellet cooled and work quickly to prevent condensation of water. Transfer the pellet with a pre-cooled spatula to a screw-crap tube with Extraction Mixture
6.Mix the cell pellet thoroughly with Extraction Mixture by shaking by hand
7.Freeze the tube immediately in liquid nitrogen
8.Break cells in the Savant FastPrep FP120. Three times 40 seconds at speed 4.0 (cool cells between steps if necessary)
9.Centrifuge for 5 minutes at 4°C in an Eppendorf centrifuge at 10.000 rpm
10.Transfer 500 µl of the supernatant to a new tube. Add 400 µl chloroform (chloroform should be cooled at 4°C)
11.Centrifuge for 2 minutes in an Eppendorf centrifuge at full speed (4°C)
5.Continue with the "High Pure RNA Isolation Kit" from Roche (order # 1 828 665)
6.Incubate for 60 minutes with DnaseI, elute with 50 µl elution buffer
7.Store the RNA in at least 2 aliquots, one of 20 µl (for concentration and quality analysis and labeling) and one back-up of 30 µl at 80°C.
|
| Label |
Cy5
|
| Label protocol |
cDNA synthesis and Labeling Protocol 1.4
Annealing Annealing Mix
x µl RNA preparation (=10 µg)
y µl nuclease-free water
1 µl Random Nonamers
11 µl TOTAL
1.mix Annealing Mix in a 200 µl PCR tube gently by pipetting up and down
2.incubate for 5’ 70°C
3.cool at room temperature for 10’ (annealing)
4.spin down the mixture to the bottom of the tube
5.place on ice Reverse transcription
Reverse Transcription Mix
4 µl 5x buffer
2 µl 0.1 M DTT
1 µl dNTP-mix
1 µl AA-dUTP
1 µl TMIII (keep only briefly outside 20°C)
20 µl TOTAL
1.Mix by very gently by pipetting up and down.
2.Incubate for 3 hrs at 42°C (in PCR-machine)
3.Cool on ice for immediate purification or place at 20°C for storage
Degradation of mRNA
1.Add 2 µl 2,5 M NaOH
2.Mix (vortex) and spin down
3.Incubate for 15 min. at 37°C
4.Add 10 µl 2 M HEPES free acid
5.Mix (vortex) and spin down
6.Ready for purification or store at 20°C
Labelling of cDNA with cyanine dyes Purification of amino allyl-modified cDNA Followed Ge Healthcare kit "Amersham CyDye (Cy3/Cy5)Reactive Dye Protocols for Post Labelling Aminoallyl-cDNA and Aminoallyl-aRNA" code RPN5661
Labelling of amino allyl-modified cDNA with CyDye
1.Add the amino allyl modified cDNA (in 0.1 M sodium bicarbonate) directly into one aliquot of CyDye NHS Ester. Resuspend the ester completely by pipetting several times and transfer the solution to an amber 1.5 ml tube
2.Incubate at room temperature, in the dark for 60 to 90 minutes
3.Add 15 µl 4 M Hydroxylamine to each coupling reaction
4.Mix by stirring and incubate at room temperature, in the dark, for 15 minutes
5.Proceed directly to purification of CyDye-labelled cDNA following Ge Healthcare kit "Amersham CyDye (Cy3/Cy5)Reactive Dye Protocols for Post Labelling Aminoallyl-cDNA and Aminoallyl-aRNA" product code RPN5661
|
| |
|
| |
| Hybridization protocol |
Agilent hybridization protocol version 4.1
|
| Scan protocol |
Scanning protocol. Using the Scan Array Express microarray scanner.
1.Turn on the scanner and the computer (in this order)
2.Login: scanner
3.Double click the 'ScanArray Express' icon
4.Switch on lasers 1 and 3 at least 15 minutes prior to scanning arrays
5.Click the 'File' button This is to prevent you from accidentally turning off the laser after the 15 minutes warming-up phase
6.Insert the slide with the array-side up and the label towards the outside. On Agilent slides the array side is the side with the label that has the word "Agilent" on it
7.Press 'Scan | Prescan'
8.Put resolution at 50 m, select both labels used, and set PMT values for both channels at for instance 40% (Agilent arrays)
9.Press 'Start'
10.Press 'Palette,' 'Green' as soon as projection of the image has started (first dye), select the red colour as soon as scanning of the second layer (second dye) has started
11.Adjust PMT values to balance signals obtained for both channels. If necessary do a few low-resolution scans to obtain a optimal balance
12.Click the 'Scan' button again
13.Select frame for high resolution scan, adjust resolution (to 10 m) and scan the array for both dyes
14.Press 'File | Save' to save the files, 'Save all' saves both dye layers "Create a new folder for each array "'Save all' saves the signals from both layers in individual files
15.Switch off the lasers and the scanner.
|
| Description |
NZ7603_vs_WCFS1
|
| Data processing |
Data Processing 1.- Background correction 2.-Normalization lowess.
|
| |
|
| Submission date |
Aug 10, 2007 |
| Last update date |
Aug 14, 2011 |
| Contact name |
L. Mariela Serrano |
| Organization name |
TI Food and Nutrition
|
| Street address |
Nieuwe Kanaal 9A
|
| City |
Wageningen |
| ZIP/Postal code |
6709 PA |
| Country |
Netherlands |
| |
|
| Platform ID |
GPL4318 |
| Series (1) |
| GSE8744 |
Heme_k2_Filtered bckg correct trans-norm |
|
| Data table header descriptions |
| ID_REF |
Spot identifier, references platform spot identifier |
| PROBE |
Probe name, references platform spot identifier by name |
| SIGNAL_CH1 |
|
| SIGNAL_CH2 |
|
| VALUE |
Log2 of ratio (Channel1 normalized signal/Channel2 normalized signal) |
| F_CH1_MEAN |
Channel1 mean of spot pixel intensities |
| B_CH1_MEAN |
Channel1 mean of spot background pixel intensities |
| F_CH2_MEAN |
Channel2 mean of spot pixel intensities |
| B_CH2_MEAN |
Channel2 mean of spot background pixel intensities |
