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PMID: 6641475 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

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

DNA (Mary Ann Liebert, Inc.) ·Vol. 2 ·No. 3 ·1983-00-00 ·Pages 243-54

Bresser J, Doering J, Gillespie D

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.

MeSH Terms
Cells/analysis Collodion DNA/isolation & purification DNA, Bacterial/isolation & purification DNA, Viral/isolation & purification HeLa Cells Humans Methods Nucleic Acid Hybridization RNA, Messenger/isolation & purification Sodium Iodide
Chemicals
DNA, Bacterial DNA, Viral RNA, Messenger Collodion DNA Sodium Iodide
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Bresser J
Doering J
Gillespie D
Article Info
Journal
DNA (Mary Ann Liebert, Inc.)
Abbr.
DNA
ISSN
0198-0238
Published
1983-00-00
Pages
243-54
Language
English
Region
United States
NLM ID
8302432
Subset
IM
Grants
NIGMS NIH HHS · GM27270 · United States
NICHD NIH HHS · HD13860 · United States
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