Literature DB >> 6641475

Quick-blot: selective mRNA or DNA immobilization from whole cells.

J Bresser, J Doering, D Gillespie.   

Abstract

Quick-blot, a method for selectively immobilizing either mRNA or DNA on nitrocellulose, is described in detail. Essential elements of the procedure for immobilizing DNA include tissue lysis, proteinase K treatment, solubilization of nucleic acids in hot 12.2 molal NaI, passage through a nitrocellulose filter, and acetylation of residual protein with acetic anhydride. Advantages include speed, quantitative recovery, low background, and elimination of the usual baking step. Essential elements of the procedure for selectively immobilizing mRNA include dissolving cells in Brij-35 and desoxycholate, proteinase K treatment, solubilizing nucleic acids in room temperature 12.2 molal NaI, filtration through nitrocellulose, and acetylation of residual protein. Advantages include selective immobilization of mRNA but not tRNA, rRNA, or DNA, and the maintenance of biological activity of the immobilized mRNA. Control experiments to optimize the procedures and examples of their application are shown.

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Year:  1983        PMID: 6641475     DOI: 10.1089/dna.1983.2.243

Source DB:  PubMed          Journal:  DNA        ISSN: 0198-0238


  24 in total

1.  Mutagenesis of the in-frame opal termination codon preceding nsP4 of Sindbis virus: studies of translational readthrough and its effect on virus replication.

Authors:  G P Li; C M Rice
Journal:  J Virol       Date:  1989-03       Impact factor: 5.103

2.  Linear- and circular-plasmid copy numbers in Borrelia burgdorferi.

Authors:  J Hinnebusch; A G Barbour
Journal:  J Bacteriol       Date:  1992-08       Impact factor: 3.490

3.  Characterization of sublines of Epstein-Barr virus producing HR-1 cells and its implication in virus propagation in culture.

Authors:  G Q Yao; C H Tsai; Y C Cheng
Journal:  Virus Genes       Date:  1995-02       Impact factor: 2.332

4.  Limited expression of poliovirus by vaccinia virus recombinants due to inhibition of the vector by proteinase 2A.

Authors:  J E Jewell; L A Ball; R Rueckert
Journal:  J Virol       Date:  1990-03       Impact factor: 5.103

5.  Characterization of the rat Class 3 aldehyde dehydrogenase gene promoter.

Authors:  Y Q Xie; K Takimoto; H C Pitot; W K Miskimins; R Lindahl
Journal:  Nucleic Acids Res       Date:  1996-11-01       Impact factor: 16.971

6.  Intracellular location of rabbit poxvirus nucleic acid within infected cells as determined by in situ hybridization.

Authors:  H Minnigan; R W Moyer
Journal:  J Virol       Date:  1985-09       Impact factor: 5.103

7.  A fast and sensitive method for detecting specific viral RNA in mammalian cells.

Authors:  U Paeratakul; P R De Stasio; M W Taylor
Journal:  J Virol       Date:  1988-04       Impact factor: 5.103

8.  An in vitro model of allergen-dependent IgE synthesis by human B lymphocytes: comparison of the response of an atopic and a non-atopic individual to Dermatophagoides spp. (house dust mite).

Authors:  R E O'Hehir; V Bal; D Quint; R Moqbel; A B Kay; E D Zanders; J R Lamb
Journal:  Immunology       Date:  1989-04       Impact factor: 7.397

9.  Transformation of T-lymphocyte subsets by Marek's disease herpesvirus.

Authors:  K A Schat; C L Chen; B W Calnek; D Char
Journal:  J Virol       Date:  1991-03       Impact factor: 5.103

10.  Potent inhibition of Epstein-Barr virus by phosphorothioate oligodeoxynucleotides without sequence specification.

Authors:  G Q Yao; S Grill; W Egan; Y C Cheng
Journal:  Antimicrob Agents Chemother       Date:  1993-07       Impact factor: 5.191

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