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Sample GSM3397301 Query DataSets for GSM3397301
Status Public on Jun 19, 2019
Title SIHA ALDH -ve
Sample type RNA
 
Source name Cell line
Organism Homo sapiens
Characteristics disease state: Cervical cancer
gender: Female
Treatment protocol Sorted the cells with Flow cytometry with ALDH and CD133 antibody
Growth protocol Cells Cultured in DMEM-F12 media (Invitrogen, USA) and 10%FBS (USA origin), at 37C in 5%CO2 till 70%confluency
Extracted molecule total RNA
Extraction protocol The RNA extraction from the samples was performed by Qiagen RNeasy Mini Kit with DNAse treatment (Cat.No. 74004) as per manufacturer’s protocol.
Label Cy3
Label protocol The samples for Gene expression were labeled using Agilent Quick-Amp labeling Kit (p/n5190-0442). 500ng each of total RNA were reverse transcribed at 40°C using oligo dT primer tagged to a T7 polymerase promoter and converted to double stranded cDNA. Synthesized double stranded cDNA were used as template for cRNA generation. cRNA was generated by in vitro transcription and the dye Cy3 CTP(Agilent) was incorporated during this step. The cDNA synthesis and in vitro transcription steps were carried out at 40°C. Labeled cRNA was cleaned up using Qiagen RNeasy columns (Qiagen, Cat No: 74106) and quality assessed for yields and specific activity using the Nanodrop ND-1000.
 
Hybridization protocol 600ng of labeled cRNA sample were fragmented at 60 º C and hybridized on to a Agilent's human GXP_8X60k Array . (AMADID: 039494). Fragmentation of labeled cRNA and hybridization were done using the Gene Expression Hybridization kit of (Agilent Technologies, In situ Hybridization kit, Part Number 5190-0404). Hybridization was carried out in Agilent’s Surehyb Chambers at 65º C for 16 hours.
Scan protocol Agilent Microarray Scanner (Agilent Technologies, Part Number G2600D).
Description Gene expression after sorting cells
Data processing Images were quantified using Feature Extraction Software ( Agilent). Feature extracted raw data was analyzed using GeneSpring GX software from Agilent. Normalization of the data was done in GeneSpring GX using the percentile shift normalization method .
 
Submission date Sep 20, 2018
Last update date Jun 19, 2019
Contact name Shifa Javed
E-mail(s) shifajvd@gmail.com
Organization name Postgraduate Institute of Medical Education and Research
Department Cytology and GynecPathology
Lab Molecular Pathology
Street address Sector 12, Chandigarh, India
City Chandigarh
State/province Outside US
ZIP/Postal code 160012
Country India
 
Platform ID GPL17077
Series (1)
GSE120270 Gene expression profiling of the cancer stem cells of cervical cancer vs the bulk population

Data table header descriptions
ID_REF
VALUE Log base 2

Data table
ID_REF VALUE
A_19_P00315452 -5.0614424
A_19_P00315459 -2.7335105
A_19_P00315482 -6.759956
A_19_P00315492 -5.4708285
A_19_P00315493 -1.8022361
A_19_P00315502 -4.739734
A_19_P00315506 -1.0472789
A_19_P00315518 -7.6835084
A_19_P00315519 -7.7076235
A_19_P00315524 -2.2037268
A_19_P00315528 -3.4328704
A_19_P00315529 -3.4626799
A_19_P00315538 -7.655713
A_19_P00315541 -7.166086
A_19_P00315543 -4.070208
A_19_P00315550 1.1071329
A_19_P00315551 0.23842049
A_19_P00315554 -7.278411
A_19_P00315581 2.507783
A_19_P00315583 -2.970532

Total number of rows: 50599

Table truncated, full table size 1184 Kbytes.




Supplementary file Size Download File type/resource
GSM3397301_SG13134300_253949437184_S001_GE1_1105_Oct12_1_2.txt.gz 12.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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