[Cloning differentially expressed genes by suppression subtractive hybridization in rat liver regeneration].
Yuchang Li, Cunshuan Xu, Yunhan Zhang
Abstract
Yuchang Li, Cunshuan Xu, Yunhan Zhang
Abstract
The cDNA from rat regenerating liver tissue was used as the tester and that from normal liver was used as the driver. A highly efficient subtractive cDNA library was constructed by suppression subtractive hybridization(SSH). After screening, 31 clones from 50 clones which were derived from the cDNA library were inserted by 60-400 bp cDNA fragments. 24 cDNA fragments corresponded to known genes and 7 cDNA fragments were unknown sequences (GenBank accession number: BG447490-447496).
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The cDNA from rat regenerating liver tissue was used as the tester and that from normal liver was used as the driver. A highly efficient subtractive cDNA library was constructed by suppression subtractive hybridization(SSH). After screening, 31 clones from 50 clones which were derived from the cDNA library were inserted by 60-400 bp cDNA fragments. 24 cDNA fragments corresponded to known genes and 7 cDNA fragments were unknown sequences (GenBank accession number: BG447490-447496).
Key concepts: Suppression subtractive hybridization, Complementary DNA, Biology, cDNA library, GenBank, Cloning (programming), Molecular biology, Gene