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Sample GSM988519 Query DataSets for GSM988519
Status Public on Oct 02, 2012
Title vehicle_replicate1_PE
Sample type SRA
 
Source name vehicle_replicate1_PE
Organism Mus musculus
Characteristics grafting: A549-luc-C8
strain: SCID-beige
gender: female
Treatment protocol Animals were weighed and engrafted (day 0). Treatment was conducted on days 0,2,4,7,9. Injections of 120 nmol Py-Im polyamide in 200 uL PBS/DMSO (4:1) were performed subcutaneously. Animals were weighed again on day 6, typically not exhibiting weight loss of more then 10 %, imaged on day 10, sacrificed and tumors harvested.
Growth protocol RPMI medium supplemented with 10%FBS and Pen-Strep
Extracted molecule total RNA
Extraction protocol Experiments were performed in female SCID-beige mice (Charles River) between 8 and 12 weeks of age. Cells were injected into the left flank area of the animals as suspensions of 25 x 106 mL-1 in RPMI, 200 µL per injection. Treatment and tumor proliferation monitoring. Mice were treated following the schedule delineated in Supporting Information (Table S1). Tumor proliferation was monitored using the XENOGEN imaging device. The animals were anesthetized with 2 5 % isoflurane and subsequently transferred to the imaging chamber, whereupon the isoflurane levels were reduced to 1-2.5 %. The floor of the imager was heated to +37 ºC to avoid hypothermia. Breathing frequency was monitored and not allowed to drop below 1 s-1, adjusting the isoflurane levels accordingly at all times. Endpoint criteria and euthanasia. Animal endpoint criteria encompassed weight loss of over 15 %, restriction of motor function by the engrafted tumor, dehydration of over 10 % and moribund behavior. Where appropriate, the animals were euthanized by asphyxiation in a CO2 chamber. Tumor tissue harvest. Animals were resected and tumors excised using standard forceps, scissors and surgical blades. The tumors were combined into one sample per condition and mechanically sheared in TRIZOL, employing a specialized device (tissue tearer, model 985370). Total RNA workup was performed following the standard TRIZOL procedure, followed by a DNAse digest, double poly-A select; libraries prepared using standard Illumina reagents and protocols
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description A549-luc-C8
processed_DESeq
Data processing Bowtie mapping to hg19+mm9 transcriptome, then eXpress, then DESeq
 
Submission date Aug 20, 2012
Last update date May 15, 2019
Contact name Jevgenij A. Raskatov
E-mail(s) raskatov@caltech.edu
Phone 6263956084
Organization name CalTech
Department CCE
Lab Dervan
Street address 1200 EAST CALIFORNIA BOULEVARD
City PASADENA
State/province California
ZIP/Postal code 91125
Country USA
 
Platform ID GPL13112
Series (1)
GSE40218 Gene Expression Changes in a Tumor Xenograft by a Py-Im Polyamide
Relations
SRA SRX179415
BioSample SAMN01121004

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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