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DOP-vector PCR: a method for rapid isolation and sequencing of insert termini from PAC clones.

Name: DOP-vector PCR: a method for rapid isolation and sequencing of insert termini from PAC clones.
Creator: Oxford University Press
Published: 1996-07-01T00:00:00+08:00

PubMed Central1996-07-01 更新2026-05-25 收录

PAC克隆末端测序

基因组物理图谱构建

数据链接：

https://pmc.ncbi.nlm.nih.gov/articles/PMC145969/数据链接链接失效反馈

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DOP-vector PCR: a method for rapid isolation and sequencing of insert termini from PAC clones.

应用场景：

提供机构：

Oxford University Press

创建时间：

1996-07-01

免疫信号传导

受体样激酶

A cDNA encoding a chitinase-related receptor-like kinase, designated CHRK1, was isolated from tobacco (Nicotiana tabacum). The C-terminal kinase domain (KD) of CHRK1 contained all of the conserved ami

PubMed Central40

The Ogg1 protein of Saccharomyces cerevisiae: a 7,8-dihydro-8-oxoguanine DNA glycosylase/AP lyase whose lysine 241 is a critical residue for catalytic activity.

DNA损伤修复

催化机制分析

The OGG1 gene of Saccharomyces cerevisiae codes for a DNA glycosylase that excises 7,8-dihydro-8- oxoguanine (8-OxoG) and 2,6-diamino-4-hydroxy-5- N -methylformamidopyrimidine (Fapy) from damaged DNA.

PubMed Central1997-08-15 更新20

Rapid preparation of single stranded DNA from PCR products by streptavidin induced electrophoretic mobility shift.

单链DNA制备

PCR产物纯化

Streptavidin induced electrophoretic mobility shift was used to prepare single stranded (ss) DNA amplified with the polymerase chain reaction in the presence of a biotinylated and a non-biotinylated p

PubMed Central1996-09-15 更新10

Database on the structure of large subunit ribosomal RNA.

RNA病毒系统发育

RNA二级结构比对

The Antwerp database on large subunit ribosomal RNA now contains 607 complete or nearly complete aligned sequences. The alignment incorporates secondary structure information for each sequence. Other

PubMed Central1999-01-01 更新20

Differential Regulation of a Family of Apyrase Genes from Medicago truncatula

豆科-根瘤菌共生结瘤

结瘤基因表达调控

Four putative apyrase genes were identified from the model legume Medicago truncatula. Two of the genes identified from M. truncatula (Mtapy1 and Mtapy4) are expressed in roots and are inducible withi

PubMed Central20

DOP-vector PCR: a method for rapid isolation and sequencing of insert termini from PAC clones.

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