Reference - Detail
| RRC ID | 73452 |
|---|---|
| Author | Kato S, Ohtoko K, Ohtake H, Kimura T. |
| Title | Vector-capping: a simple method for preparing a high-quality full-length cDNA library. |
| Journal | DNA Res |
| Abstract |
Full-length cDNAs play an essential role in identifying genes and determining their promoter regions. Here we describe a simple method for constructing a full-length cDNA library, which has the following advantages: (i) it consists of only three steps including direct ligation between a vector and a cDNA strand using T4 RNA ligase, (ii) it contains neither a PCR process generating mutations nor restriction enzyme treatment causing truncation of cDNA, (iii) the intactness of cDNA is assured due to the presence of an additional dGMP at its 5' end, (iv) approximately 95% of cDNA clones are full-length when cultured cells or fresh tissues are used, (v) several micrograms of total RNA without mRNA purification is sufficient for preparation of a library containing >10(5) independent clones, and (vi) a long-sized full-length cDNA up to 9.5 kbp can be cloned. This method will accelerate comprehensive gene analysis in a variety of eukaryotes. |
| Volume | 12(1) |
| Pages | 53-62 |
| Published | 2005-2-28 |
| DOI | 10.1093/dnares/12.1.53 |
| PMID | 16106752 |
| MeSH | Animals Base Sequence Cell Line Cells, Cultured Gene Library* Genetic Vectors Humans Mice Molecular Sequence Data Nucleotides / metabolism RNA Caps / metabolism* RNA, Messenger Reverse Transcriptase Polymerase Chain Reaction |
| IF | 4.009 |
| Altmetric score |
オルトメトリクス指標項目
|
| The most frequently cited source | Patent(IFI CLAIMS) |
| Total number of mentions | 12 |
| Altmetric score changes over past 6months | 0.0 |
| Resource | |
| DNA material | NRCD human cDNA clones (RDB06607) |