CLC number: S482.3+3
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
Crosschecked: 2016-01-06
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Citations: Bibtex RefMan EndNote GB/T7714
Hong-cui Liu, Bing-qiang Yuan, Shao-nan Li. Developing antibodies from cholinesterase derived from prokaryotic expression and testing their feasibility for detecting immunogen content in Daphnia magna[J]. Journal of Zhejiang University Science B, 2016, 17(2): 110-126.
@article{title="Developing antibodies from cholinesterase derived from prokaryotic expression and testing their feasibility for detecting immunogen content in Daphnia magna",
author="Hong-cui Liu, Bing-qiang Yuan, Shao-nan Li",
journal="Journal of Zhejiang University Science B",
volume="17",
number="2",
pages="110-126",
year="2016",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B1500008"
}
%0 Journal Article
%T Developing antibodies from cholinesterase derived from prokaryotic expression and testing their feasibility for detecting immunogen content in Daphnia magna
%A Hong-cui Liu
%A Bing-qiang Yuan
%A Shao-nan Li
%J Journal of Zhejiang University SCIENCE B
%V 17
%N 2
%P 110-126
%@ 1673-1581
%D 2016
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B1500008
TY - JOUR
T1 - Developing antibodies from cholinesterase derived from prokaryotic expression and testing their feasibility for detecting immunogen content in Daphnia magna
A1 - Hong-cui Liu
A1 - Bing-qiang Yuan
A1 - Shao-nan Li
J0 - Journal of Zhejiang University Science B
VL - 17
IS - 2
SP - 110
EP - 126
%@ 1673-1581
Y1 - 2016
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B1500008
Abstract: To yield cholinesterase (ChE) from prokaryotic expression, the ChE gene that belongs to Daphnia magna was amplified by reverse transcription-polymerase chain reaction (RT-PCR) using forward primer 5'-CCCYGGNGCSAT GATGTG-3' and reverse primer 5'-GYAAGTTRGCCCAATATCT-3'. To express the gene, one sequence of the amplified DNA, which was able to encode a putative protein containing two conserved carboxylesterase domains, was connected to the prokaryotic expression vector PET-29a(+). The recombinant vector was transformed into Escherichia coil BL21 (DE3). Protein expression was induced by isopropy-
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