T-linker-specific ligation PCR (T-linker PCR): an advanced PCR technique for chromosome walking or for isolation of tagged DNA ends.
about
SiteFinding-PCR: a simple and efficient PCR method for chromosome walking.Current and new approaches in GMO detection: challenges and solutionsHemi-nested touchdown PCR combined with primer-template mismatch PCR for rapid isolation and sequencing of low molecular weight glutenin subunit gene family from a hexaploid wheat BAC libraryRestriction site-dependent PCR: an efficient technique for fast cloning of new genes of microorganismsAn enhanced method for sequence walking and paralog mining: TOPO(R) Vector-Ligation PCR.Fusion primer and nested integrated PCR (FPNI-PCR): a new high-efficiency strategy for rapid chromosome walking or flanking sequence cloningSequencing, identification and mapping of primed L1 elements (SIMPLE) reveals significant variation in full length L1 elements between individualsMolecular characterization of transgene integration by next-generation sequencing in transgenic cattle.Partially overlapping primer-based PCR for genome walking.Identification of the Genomic Insertion Site of the Thyroid Peroxidase Promoter-Cre Recombinase Transgene Using a Novel, Efficient, Next-Generation DNA Sequencing Method.Self-formed adaptor PCR: a simple and efficient method for chromosome walking.The Nucleotide Excision Repair Pathway Limits L1 RetrotranspositionRetroviral insertional mutagenesis: past, present and future.Characterization of bacterial operons consisting of two tubulins and a kinesin-like gene by the novel Two-Step Gene Walking method.Randomly broken fragment PCR with 5' end-directed adaptor for genome walking.Genome walking in eukaryotes.DNA enrichment approaches to identify unauthorized genetically modified organisms (GMOs).Isolation and characterization of Histone1 gene and its promoter from tea plant (Camellia sinensis).Linear and exponential TAIL-PCR: a method for efficient and quick amplification of flanking sequences adjacent to Tn5 transposon insertion sites.Transcription coupled repair and biased insertion of human retrotransposon L1 in transcribed genes.The increased expression of follicle-stimulating hormone leads to a decrease of fecundity in transgenic Large White female pigs.Stepwise partially overlapping primer-based PCR for genome walking.
P2860
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P2860
T-linker-specific ligation PCR (T-linker PCR): an advanced PCR technique for chromosome walking or for isolation of tagged DNA ends.
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
T-linker-specific ligation PCR ...... isolation of tagged DNA ends.
@ast
T-linker-specific ligation PCR ...... isolation of tagged DNA ends.
@en
type
label
T-linker-specific ligation PCR ...... isolation of tagged DNA ends.
@ast
T-linker-specific ligation PCR ...... isolation of tagged DNA ends.
@en
prefLabel
T-linker-specific ligation PCR ...... isolation of tagged DNA ends.
@ast
T-linker-specific ligation PCR ...... isolation of tagged DNA ends.
@en
P2093
P2860
P356
P1476
T-linker-specific ligation PCR ...... isolation of tagged DNA ends.
@en
P2093
An Chengcai
Chen Zhangliang
Tan Guihong
Yan Yuanxin
P2860
P356
10.1093/NAR/GNG068
P407
P577
2003-06-01T00:00:00Z