Literature DB >> 9893748

Rapid and effective processing of blood specimens for diagnostic PCR using filter paper and Chelex-100.

J M Polski1, S Kimzey, R W Percival, L E Grosso.   

Abstract

AIM: To provide a more efficient method for isolating DNA from peripheral blood for use in diagnostic DNA mutation analysis.
METHODS: The use of blood impregnated filter paper and Chelex-100 in DNA isolation was evaluated and compared with standard DNA isolation techniques.
RESULTS: In polymerase chain reaction (PCR) based assays of five point mutations, identical results were obtained with DNA isolated routinely from peripheral blood and isolated using the filter paper and Chelex-100 method.
CONCLUSION: In the clinical setting, this method provides a useful alternative to conventional DNA isolation. It is easily implemented and inexpensive, and provides sufficient, stable DNA for multiple assays. The potential for specimen contamination is reduced because most of the steps are performed in a single microcentrifuge tube. In addition, this method provides for easy storage and transport of samples from the point of acquisition.

Mesh:

Substances:

Year:  1998        PMID: 9893748      PMCID: PMC395639          DOI: 10.1136/mp.51.4.215

Source DB:  PubMed          Journal:  Mol Pathol        ISSN: 1366-8714


  14 in total

1.  Direct PCR from whole blood, without DNA extraction.

Authors:  B Mercier; C Gaucher; O Feugeas; C Mazurier
Journal:  Nucleic Acids Res       Date:  1990-10-11       Impact factor: 16.971

2.  Isolation of DNA from blood.

Authors:  T L Kendall; D J Byerley; R Dean
Journal:  Anal Biochem       Date:  1991-05-15       Impact factor: 3.365

3.  A rapid method for preparing DNA from blood, suited for PCR screening of transgenes in mice.

Authors:  G Winberg
Journal:  PCR Methods Appl       Date:  1991-08

4.  Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material.

Authors:  P S Walsh; D A Metzger; R Higuchi
Journal:  Biotechniques       Date:  1991-04       Impact factor: 1.993

5.  A one-step microbial DNA extraction method using "Chelex 100" suitable for gene amplification.

Authors:  X de Lamballerie; C Zandotti; C Vignoli; C Bollet; P de Micco
Journal:  Res Microbiol       Date:  1992-10       Impact factor: 3.992

6.  A nontoxic and versatile protein salting-out method for isolation of DNA.

Authors:  J Laitinen; J Samarut; E Hölttä
Journal:  Biotechniques       Date:  1994-08       Impact factor: 1.993

7.  DNA microextraction from dried blood spots on filter paper blotters: potential applications to newborn screening.

Authors:  E R McCabe; S Z Huang; W K Seltzer; M L Law
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132

8.  A simple and efficient non-organic procedure for the isolation of genomic DNA from blood.

Authors:  J Grimberg; S Nawoschik; L Belluscio; R McKee; A Turck; A Eisenberg
Journal:  Nucleic Acids Res       Date:  1989-10-25       Impact factor: 16.971

9.  A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase.

Authors:  P Frosst; H J Blom; R Milos; P Goyette; C A Sheppard; R G Matthews; G J Boers; M den Heijer; L A Kluijtmans; L P van den Heuvel
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10.  Determination of genetic variation within Plasmodium falciparum by using enzymatically amplified DNA from filter paper disks impregnated with whole blood.

Authors:  K C Kain; D E Lanar
Journal:  J Clin Microbiol       Date:  1991-06       Impact factor: 5.948

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  15 in total

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Journal:  BMC Res Notes       Date:  2012-09-13

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9.  Failure to detect Plasmodium vivax in West and Central Africa by PCR species typing.

Authors:  Richard L Culleton; Toshihiro Mita; Mathieu Ndounga; Holger Unger; Pedro V L Cravo; Giacomo M Paganotti; Nobuyuki Takahashi; Akira Kaneko; Hideaki Eto; Halidou Tinto; Corine Karema; Umberto D'Alessandro; Virgilio do Rosário; Takatoshi Kobayakawa; Francine Ntoumi; Richard Carter; Kazuyuki Tanabe
Journal:  Malar J       Date:  2008-09-11       Impact factor: 2.979

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