Pre-PCR Gel-Loading Buffer that Increases Specificity

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چکیده

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منابع مشابه

Pre-PCR gel-loading buffer that increases specificity.

of DNA melting curves during the polymerase chain reaction. Anal. Biochem. 245:154-160. 7.Trka, J., V. Divoky, and T. Lion. 1995. Prevention of product carry-over by single tube two-round (ST-2R) PCR: application to BCRABL analysis in chronic myelogenous leukemia. Nucleic Acids Res. 23:4736-4737. 8.Wittwer, C.T., K.M. Ririe, R.V. Andrew, D.A. David, R.A. Gundry and U.J. Balis. 1997. The LightCy...

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Because of its simplicity, PCR performed directly from bacterial colonies on agar plates has been extensively used as a first step in the identification of recombinant clones (1–3,6,7). Instead of making DNA minipreps and restriction digestion from several putative recombinant colonies, colony PCR allows the identification of the positive clones, and so reduces these procedures to one clone per...

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Enhanced sensitivity RNA gel loading buffer that enables efficient RNA separation on native gels.

RNA gel analysis is essential for quality assessment of RNA preparations for subsequent analysis such as microarrays and real-time PCRs. The routinely used standard electrophoresis of RNA through formaldehyde-containing agarose gels is not only labor-intensive and time-consuming, but also involves sizeable quantities of hazardous materials. Above all, it is not sensitive, requiring more than 1 ...

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Maximizing sensitivity and specificity of PCR by pre-amplification heating

We have found that assembling the reaction mixture at a temperature greater than the annealing temperature improved both product yield and specificity of PCR. When reactions were maintained at 70°C in a dry heating block during addition of denatured samples to aliquotted reagent master mix, a reproducible increase in product yield was observed compared to duplicates maintained at room temperatu...

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Useful buffer and gel systems for polyacrylamide gel electrophoresis.

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ژورنال

عنوان ژورنال: BioTechniques

سال: 2000

ISSN: 0736-6205,1940-9818

DOI: 10.2144/00294bm02