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Cancer Genome Characterization Initiative

Visit the database of genomic characterization data for multiple tumor types.


Library Info Page


Library ID

Library Name:S2SNU668s1
Organism:Homo sapiens
UniGene Library ID:10296
Tissue Description:
Library Keywords:metastasis, cell line, adult, subtracted, ascites, EST, plasmid vector, stomach cancer

Clones and Sequences

#Clones Generated to Date:
#Sequences Generated to Date:1875

Library Preparation Details

Description:The poly (A)+ RNA was decapped with tabacco acid pyrophosphatase (TAP) and ligated with DNA-RNA linker including EcoRI site by treatment of T4 RNA ligase. The first strand cDNA was synthesized from oligo dT-selected mRNA by priming with dT-tailed vector. The dT-tailed vector was adjusted to have about 60nt. The cDNA vector was circularized with E. coli DNA ligase after digestion of EcoRI which site is also included in vector. An RNA strand converted to a DNA strand by Okayama-Berg method. The obtained cDNA vectors were used for transformation of competent cells E. coli Top10F' by electroporation method. After analyzing and sequencing about 2,000 ~ 3,000 colonies in original cDNA library, the abundant cDNAs were selected and amplified by PCR reaction using vector region primer including T7 promotor as 5' primer and N(dT)14 as 3' primer. The PCR products were used as template for synthesis of biotinylated single stranded RNA by in vitro transcription reaction. The synthesized RNA probes were hybridized with antisense single stranded cDNAs prepared from original liberary and incubated with avidin-gel. After removing DNA-RNA hybrids by centrifuge, the subtracted cDNA libraries were constructed by transformaion of the remaining DNA into competent cells E. coli Top10F' with electroporation method.
R. Site1:EcoRI
R. Site2:NotI
Lab Host:Top10F'
Vector:pCNS
Vector Type:Plasmid
Tissue Supplier:
Library Producer: