Methodology for Detecting Trace Amounts of Microchimeric DNA from Peripheral Murine White Blood Cells by Real-Time PCR

<p>Real-time PCR methodology can successfully quantitate microchimeric cell populations at a concentration of 100 microchimeric cells/100,000 host cells; however, it has not been successful in quantitating DNA from trace numbers of microchimeric white blood cells which we reported are present...

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Bibliographic Details
Main Authors: Artlett Carol M., Dito C. Gennaro, Christner Paul J.
Format: Article
Language:English
Published: BMC 2003-01-01
Series:Biological Procedures Online
Subjects:
DNA
Online Access:http://www.biologicalprocedures.com/bpo/arts/1/51/m51.htm
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spelling doaj-a41d5f7a6570421e814d4b6c9d57bd122020-11-24T21:28:38ZengBMCBiological Procedures Online1480-92222003-01-015110310710.1251/bpo51Methodology for Detecting Trace Amounts of Microchimeric DNA from Peripheral Murine White Blood Cells by Real-Time PCR Artlett Carol M.Dito C. GennaroChristner Paul J.<p>Real-time PCR methodology can successfully quantitate microchimeric cell populations at a concentration of 100 microchimeric cells/100,000 host cells; however, it has not been successful in quantitating DNA from trace numbers of microchimeric white blood cells which we reported are present in murine peripheral blood at a concentration as low as 2/100,000 host cells. We report methodology using primers for a portion of the H2-k<sup>b</sup> murine histocompatibility sequence, specific for the C57BL/6J mouse. When these primers were used in the presence of 11,000 &mgr;M primer, a 20-fold increase in the median manufacturer&rsquo;s recommended concentration, the assay could be optimized to detect 34 pg of C57BL/6J DNA in a background of 2.5 &mgr;g of carrier BALB/cJ DNA (1/100,000). These conditions resulted in a detection limit half as sensitive as that found when no carrier DNA was present.http://www.biologicalprocedures.com/bpo/arts/1/51/m51.htmPolymerase Chain ReactionDNAMiceT-Lymphocytesleukocytes
collection DOAJ
language English
format Article
sources DOAJ
author Artlett Carol M.
Dito C. Gennaro
Christner Paul J.
spellingShingle Artlett Carol M.
Dito C. Gennaro
Christner Paul J.
Methodology for Detecting Trace Amounts of Microchimeric DNA from Peripheral Murine White Blood Cells by Real-Time PCR
Biological Procedures Online
Polymerase Chain Reaction
DNA
Mice
T-Lymphocytes
leukocytes
author_facet Artlett Carol M.
Dito C. Gennaro
Christner Paul J.
author_sort Artlett Carol M.
title Methodology for Detecting Trace Amounts of Microchimeric DNA from Peripheral Murine White Blood Cells by Real-Time PCR
title_short Methodology for Detecting Trace Amounts of Microchimeric DNA from Peripheral Murine White Blood Cells by Real-Time PCR
title_full Methodology for Detecting Trace Amounts of Microchimeric DNA from Peripheral Murine White Blood Cells by Real-Time PCR
title_fullStr Methodology for Detecting Trace Amounts of Microchimeric DNA from Peripheral Murine White Blood Cells by Real-Time PCR
title_full_unstemmed Methodology for Detecting Trace Amounts of Microchimeric DNA from Peripheral Murine White Blood Cells by Real-Time PCR
title_sort methodology for detecting trace amounts of microchimeric dna from peripheral murine white blood cells by real-time pcr
publisher BMC
series Biological Procedures Online
issn 1480-9222
publishDate 2003-01-01
description <p>Real-time PCR methodology can successfully quantitate microchimeric cell populations at a concentration of 100 microchimeric cells/100,000 host cells; however, it has not been successful in quantitating DNA from trace numbers of microchimeric white blood cells which we reported are present in murine peripheral blood at a concentration as low as 2/100,000 host cells. We report methodology using primers for a portion of the H2-k<sup>b</sup> murine histocompatibility sequence, specific for the C57BL/6J mouse. When these primers were used in the presence of 11,000 &mgr;M primer, a 20-fold increase in the median manufacturer&rsquo;s recommended concentration, the assay could be optimized to detect 34 pg of C57BL/6J DNA in a background of 2.5 &mgr;g of carrier BALB/cJ DNA (1/100,000). These conditions resulted in a detection limit half as sensitive as that found when no carrier DNA was present.
topic Polymerase Chain Reaction
DNA
Mice
T-Lymphocytes
leukocytes
url http://www.biologicalprocedures.com/bpo/arts/1/51/m51.htm
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