Literature DB >> 1705392

A small-scale plasmid preparation yielding DNA suitable for double-stranded sequencing and in vitro transcription.

K R Johnson1.   

Abstract

A small-scale plasmid preparation is described that is useful for a variety of procedures from double-stranded sequencing to in vitro transcription. No specialized equipment or reagents are required. The preparation of plasmid DNA does not require the use of RNase; instead the larger RNAs are precipitated with 2.5 M ammonium acetate. The resulting plasmid DNA is used routinely for double-stranded sequencing with the Klenow fragment of DNA polymerase and has been used for generating deletions with exonuclease III. In addition, the plasmid DNA has been used to generate transcripts with T7 RNA polymerase that translate well in reticulocyte lysate.

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Year:  1990        PMID: 1705392     DOI: 10.1016/0003-2697(90)90176-a

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  3 in total

1.  Protein engineering of the 2-haloacid halidohydrolase IVa from Pseudomonas cepacia MBA4.

Authors:  W Asmara; U Murdiyatmo; A J Baines; A T Bull; D J Hardman
Journal:  Biochem J       Date:  1993-05-15       Impact factor: 3.857

2.  Isolation of Brucella abortus ssb and uvrA genes from a genomic library by use of lymphocytes as probes.

Authors:  Y Zhu; S C Oliveira; G A Splitter
Journal:  Infect Immun       Date:  1993-12       Impact factor: 3.441

3.  E-cadherin/catenin complexes are formed cotranslationally in the endoplasmic reticulum/Golgi compartments.

Authors:  Matthew W Curtis; Keith R Johnson; Margaret J Wheelock
Journal:  Cell Commun Adhes       Date:  2008-11
  3 in total

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