DEVELOPMENT OF RECOMBINANT POSITIVE CONTROL FOR Francisella tularensis DETECTION BY Q-PCR
The aim of the work was to construct and test the recombinant positive control for F. tularensis detection by a real-time polymerase chain reaction (qPCR). The molecular TA-cloning of pTZ57_F/R plasmid ligated with tul4 gene PCR product into DH5α E. coli. The minimal detection level in qPCR was one...
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National Academy of Sciences of Ukraine and Palladin Institute of Biochemistry of the National Academy of Sciences of Ukraine.
2018-08-01
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doaj-35259dd607b746a9a5252b12e39d782f2020-11-24T21:09:58ZengNational Academy of Sciences of Ukraine and Palladin Institute of Biochemistry of the National Academy of Sciences of Ukraine.Biotechnologia Acta2410-77512410-776X2018-08-01114687210.15407/biotech11.04.068DEVELOPMENT OF RECOMBINANT POSITIVE CONTROL FOR Francisella tularensis DETECTION BY Q-PCRO. B. Zlenko0A. P. Gerilovych1National Scientific Center “Institute of Experimental and Clinical Veterinary Medicine” of the National Academy of Agrarian Sciences of Ukraine, KharkivNational Scientific Center “Institute of Experimental and Clinical Veterinary Medicine” of the National Academy of Agrarian Sciences of Ukraine, KharkivThe aim of the work was to construct and test the recombinant positive control for F. tularensis detection by a real-time polymerase chain reaction (qPCR). The molecular TA-cloning of pTZ57_F/R plasmid ligated with tul4 gene PCR product into DH5α E. coli. The minimal detection level in qPCR was one copy number per reaction. The obtained positive control was highly sensitive, specific and safe qPCR in the laboratory tularemia diagnostics.http://biotechnology.kiev.ua/images/storage/4_2018/zlenko_4_2018.pdfecombinant positive controlqPCRtularemiamolecular cloning |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
O. B. Zlenko A. P. Gerilovych |
spellingShingle |
O. B. Zlenko A. P. Gerilovych DEVELOPMENT OF RECOMBINANT POSITIVE CONTROL FOR Francisella tularensis DETECTION BY Q-PCR Biotechnologia Acta ecombinant positive control qPCR tularemia molecular cloning |
author_facet |
O. B. Zlenko A. P. Gerilovych |
author_sort |
O. B. Zlenko |
title |
DEVELOPMENT OF RECOMBINANT POSITIVE CONTROL FOR Francisella tularensis DETECTION BY Q-PCR |
title_short |
DEVELOPMENT OF RECOMBINANT POSITIVE CONTROL FOR Francisella tularensis DETECTION BY Q-PCR |
title_full |
DEVELOPMENT OF RECOMBINANT POSITIVE CONTROL FOR Francisella tularensis DETECTION BY Q-PCR |
title_fullStr |
DEVELOPMENT OF RECOMBINANT POSITIVE CONTROL FOR Francisella tularensis DETECTION BY Q-PCR |
title_full_unstemmed |
DEVELOPMENT OF RECOMBINANT POSITIVE CONTROL FOR Francisella tularensis DETECTION BY Q-PCR |
title_sort |
development of recombinant positive control for francisella tularensis detection by q-pcr |
publisher |
National Academy of Sciences of Ukraine and Palladin Institute of Biochemistry of the National Academy of Sciences of Ukraine. |
series |
Biotechnologia Acta |
issn |
2410-7751 2410-776X |
publishDate |
2018-08-01 |
description |
The aim of the work was to construct and test the recombinant positive control for F. tularensis detection by a real-time polymerase chain reaction (qPCR). The molecular TA-cloning of pTZ57_F/R plasmid ligated with tul4 gene PCR product into DH5α E. coli. The minimal detection level in qPCR was one copy number per reaction. The obtained positive control was highly sensitive, specific and safe qPCR in the laboratory tularemia diagnostics. |
topic |
ecombinant positive control qPCR tularemia molecular cloning |
url |
http://biotechnology.kiev.ua/images/storage/4_2018/zlenko_4_2018.pdf |
work_keys_str_mv |
AT obzlenko developmentofrecombinantpositivecontrolforfrancisellatularensisdetectionbyqpcr AT apgerilovych developmentofrecombinantpositivecontrolforfrancisellatularensisdetectionbyqpcr |
_version_ |
1716756841390669824 |