Real-time PCR-based genotyping from whole blood using Taq DNA polymerase and a buffer supplemented with 1,2-propanediol and trehalose-Reference-Cited by-同舟云学术

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Real-time PCR-based genotyping from whole blood using Taq DNA polymerase and a buffer supplemented with 1,2-propanediol and trehalose

Published:2015-01 Issue: Volume:416 Page:178-182
ISSN:0022-1759
Container-title:Journal of Immunological Methods
language:en
Short-container-title:Journal of Immunological Methods

Author:

Utekal Pavol,Kocanda Lukas,Matousek Petr,Wagner Petr,Bugajev Viktor,Draber Petr

Funder

Ministry of Industry and Trade of the Czech Republic

Grant Agency of the Czech Republic

Institutional support RVO

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference15 articles.

1. Detection of factor V Leiden from a drop of blood by PCR-SSCP;Corral;Thromb. Haemost.,1996

2. Advances in understanding pathogenic mechanisms of thrombophilic disorders;Dahlback;Blood,2008

3. Multiplexed mutagenically separated PCR: simultaneous single-tube detection of the factor V R506Q (G1691A), the prothrombin G20210A, and the methylenetetrahydrofolate reductase A223V (C677T) variants;Endler;Clin. Chem.,2001

4. A rapid, simple, and humane method for submandibular bleeding of mice using a lancet;Golde;Lab Anim. (NY),2005

5. Modification of IgH PCR clonal analysis by the addition of sucrose and cresol red directly to PCR reaction mixes;Hodges;Mol. Pathol.,1997

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