A kind of m-mlv reverse transcriptase and its application
A reverse transcriptase and carrier technology, applied in the biological field, can solve the problems of expensive imported reagents, lack of reverse transcription reagents, etc., and achieve the effects of improving detection sensitivity and experimental efficiency, high continuous synthesis ability, and strong anti-suppression ability.
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Embodiment 1
[0037] Example 1: SuperRT reverse transcriptase cloning, expression purification and detection
[0038] All DNA manipulations were performed using standard techniques, particularly cloning using PCR, PCR-based mutagenesis procedures, and standard restriction digestion and ligation. All proteins were expressed in Escherichia coli, Ni-NTA resin was purchased from Qiagen, and CM resin was purchased from QE Company. The SuperRT reverse transcriptase sequence of the present invention is shown in SEQ ID No.1, by cloning it into a modified pET21 + plasmid to construct a recombinant expression plasmid, and transforming the host bacteria, purifying, identifying and storing the host bacteria after culturing; the specific method is as follows :
[0039] (1) Plasmid construction: construct the expression plasmid pET-SRTHis of the Super RT, using primer 5'-ATATA CATATG CTAAAT ATAGAAGATGAG-3' and 5'-ATATC CTCGAG TATGAGGAGGGTAGA -3'Amplified a 2035bp DNA fragment encoding SuperRT reverse...
Embodiment 2
[0045] Example 2: Detection of reverse transcription performance of purified SuperRT reverse transcriptase
[0046] The reverse transcription performance of the purified protein was tested using the extracted human total RNA as a template. After the human RNA template RT is reverse-transcribed into cDNA, use the primers ACTB primers indicating the sequence to configure the PCR reaction. The specific experimental operation is as follows:
[0047] Prepare cDNA first-strand synthesis reaction solution, each reaction includes 7 μl nuclease-free water, Super RT reaction buffer, 4 μl 2.5mM dNTP, 2 μl random primers, 1 μl SuperRT to be tested or purchased superscrip III; will be prepared Mix the cDNA first-strand synthesis reaction solution, centrifuge briefly, and divide it into PCR reaction tubes, 18 μl per tube; add 2 μl human RNA template to each of the above reaction tubes, mix well, and put it in a PCR machine at 50°C React for 10 minutes, and stop the reverse transcription r...
Embodiment 3
[0050] Embodiment 3: Detection of poultry IBV virus with SuperRT reverse transcription reaction system
[0051] Using the SuperRT reverse transcription reagent and reaction system provided by the present invention, two avian IBV coronavirus samples (RNA virus, provided by Jiangsu Huachuang Xinnuo Pharmaceutical Technology Co., Ltd., belong to attenuated strains, are not infectious and pathogenic to humans. sex) for detection, specifically including the following steps:
[0052] 1. RNA sample preparation
[0053] 1.1 Roughly handle RNA samples: Dilute 2 poultry IBV stock solutions to 10 -3 , 10 -4 , 10 -5 , 10 -6 , 10 -7 and 10 -8 Dilution gradients are crude RNA samples for subsequent RT-PCR detection operations.
[0054] 1.2 Extract RNA samples: Take 2 poultry IBV virus stocks for RNA extraction. It is recommended to use the virus nucleic acid extraction kit CWY071 of Kangwei Century Biotechnology Co., Ltd., and operate according to the instructions. The extracted RNA...
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