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Sample GSM6246181 Query DataSets for GSM6246181
Status Public on Mar 03, 2023
Title sfl1Δ_biofilm_vs_ SN76_biofilm_rep1
Sample type RNA
 
Channel 1
Source name sfl1delta/sfl1delta
Organism Candida albicans
Characteristics genotype: sfl1delta/sfl1delta
growth mode: biofilm
Growth protocol For the transcriptomic profiling an individual colony of C. albicans SN76 and sfl1Δ/sfl1Δ strains was inoculated in SDB at 37 ºC with orbital agitation (120 rev/min) overnight and then re-inoculated (at 1x105 cel/ml) in 25 ml of RPMI at pH 4 and left to grow for 24h at 37ºC and 120 rev/min orbital shake, inside Erlenmeyer flaks and microtiter plates, in order to induce planktonic and biofilm growth, respectively.
Extracted molecule total RNA
Extraction protocol The extraction of RNA from the cells was performed using the RiboPure – Yeast Kit (Life Technologies, CA), according to the manufacturer’s instructions.The concentration and purity of the extracted RNA were determined by spectrophotometry and its integrity was confirmed in an Agilent 2100 Bioanalyzer with an RNA 6000 Nano Assay (Agilent Technologies, CA).
Label Cy5
Label protocol cDNA synthesis, hybridization, and scanning were performed using the Agilent protocol for two-color Microarray-Based Gene Expression Analysis Low Input Quick Amp Labeling v6.9 (Agilent Technologies), according to the manufacturer’s instructions. One hundred nanograms of total RNA of each strain were used to synthesize labeled cDNA (with Cyanine 3-CTP and cyanine 5-CTP), using Agilent T7 Promoter Primer and T7 RNA polymerase Blend (Agilent Technologies, Cat.5190–2305).
 
Channel 2
Source name SN76
Organism Candida albicans
Characteristics genotype: SN76
growth mode: biofilm
Growth protocol For the transcriptomic profiling an individual colony of C. albicans SN76 and sfl1Δ/sfl1Δ strains was inoculated in SDB at 37 ºC with orbital agitation (120 rev/min) overnight and then re-inoculated (at 1x105 cel/ml) in 25 ml of RPMI at pH 4 and left to grow for 24h at 37ºC and 120 rev/min orbital shake, inside Erlenmeyer flaks and microtiter plates, in order to induce planktonic and biofilm growth, respectively.
Extracted molecule total RNA
Extraction protocol The extraction of RNA from the cells was performed using the RiboPure – Yeast Kit (Life Technologies, CA), according to the manufacturer’s instructions.The concentration and purity of the extracted RNA were determined by spectrophotometry and its integrity was confirmed in an Agilent 2100 Bioanalyzer with an RNA 6000 Nano Assay (Agilent Technologies, CA).
Label Cy3
Label protocol cDNA synthesis, hybridization, and scanning were performed using the Agilent protocol for two-color Microarray-Based Gene Expression Analysis Low Input Quick Amp Labeling v6.9 (Agilent Technologies), according to the manufacturer’s instructions. One hundred nanograms of total RNA of each strain were used to synthesize labeled cDNA (with Cyanine 3-CTP and cyanine 5-CTP), using Agilent T7 Promoter Primer and T7 RNA polymerase Blend (Agilent Technologies, Cat.5190–2305).
 
 
Hybridization protocol Six hundred nanograms of labelled cDNA were hybridized in the microarray. Hybridizations were carried out using Agilent gasket slides in a rotating oven for 17 h at 65°C.
Scan protocol Slides were then washed following manufacturer’s instructions and scanned in an Agilent G2565AA microarrays scanner. Probes signal values were extracted using Agilent Feature Extraction Software.
Data processing Data were normalized using median centering of signal distribution with Biometric Research Branch BRB-Array tools v3.4.o software 36. Final statistical analysis was carried out using LIMMA package in MeV software (MultiExperiment Viewer 4.8.0) 36 with a cut-off p-value of 0.1.
 
Submission date Jun 15, 2022
Last update date Mar 03, 2023
Contact name Ana Soares
E-mail(s) ana.r.soares@ua.pt
Organization name University of Aveiro
Street address Campus de Santiago
City Aveiro
ZIP/Postal code 3810
Country Portugal
 
Platform ID GPL22275
Series (1)
GSE206208 Transcriptomic regulation of acidic biofilms by Candida albicans Sfl1

Data table header descriptions
ID_REF
VALUE Lowess normalized log2 ratio (Cy5/Cy3) representing test/reference

Data table
ID_REF VALUE
CUST_1_PI362308700 0.040093333
CUST_10_PI362308700 -0.216352865
CUST_100_PI362308700 0.50737226
CUST_1000_PI362308700 0.249587312
CUST_10000_PI362308700 -1.470273256
CUST_10001_PI362308700 -0.373405576
CUST_10002_PI362308700 -0.607161999
CUST_10003_PI362308700 -0.882110715
CUST_10004_PI362308700 -0.878013253
CUST_10005_PI362308700 -0.665114105
CUST_10006_PI362308700 -0.655835092
CUST_10007_PI362308700 -0.006347936
CUST_10008_PI362308700 0.015256579
CUST_10009_PI362308700 -0.141949758
CUST_1001_PI362308700 0.08730156
CUST_10010_PI362308700 -0.21981746
CUST_10011_PI362308700 -1.166702032
CUST_10012_PI362308700 -1.103838086
CUST_10013_PI362308700 -0.164027944
CUST_10014_PI362308700 -0.393347114

Total number of rows: 12202

Table truncated, full table size 404 Kbytes.




Supplementary file Size Download File type/resource
GSM6246181_US45102846_256513810007_S01_GE2_1200_Jun14_1_1.txt.gz 1.5 Mb (ftp)(http) TXT
Processed data included within Sample table

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