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30results about How to "No need for electrophoretic detection" patented technology

Loop isothermal amplification primer for quickly detecting tylenchulus semipenetrans and application of loop isothermal amplification primer

The invention discloses a loop isothermal amplification primer for quickly detecting tylenchulus semipenetrans and application of the loop isothermal amplification primer. The loop isothermal amplification primer comprises a primer pair TSF3 / TSB3 and a primer pair TSFIP / TSBIP, and the sequences of the primer pairs are shown as SEQ ID NO. 1 to 4 respectively. A loop isothermal amplification method is established through the loop isothermal amplification primer, loop isothermal amplification is performed through taking a sample DNA as a template, and results can be judged in two ways after the end of reaction, wherein the first way is that an amplification primer is subjected to electrophoresis, and a sample of a specific ladder-shaped strip, which occurs, is judged to be positive; the second way is that through adding SYBR green I into a reaction system, a sample of which the color is changed is observed with naked eyes to be positive. The loop isothermal amplification method is low in requirement for instruments and equipment, quick, safe, and high in specificity and sensitivity; a technical support is provided for the detection of the tylenchulus semipenetrans, in particular to the quick detection work of a grass-root quarantine unit for the tylenchulus semipenetrans, and the popularization and application values are very high.
Owner:SOUTH CHINA AGRI UNIV

Real-time recombinase-mediated isothermal amplification nucleic acid kit for rapid detection of toxoplasma gondii and application thereof

The invention discloses a real-time recombinase-mediated isothermal amplification nucleic acid kit for rapid detection of toxoplasma gondii and an application thereof. The kit comprises standards. Thestandards are a positive plasmid containing a 529 gene sequence, specific primers and probes designed for 529 gene of the toxoplasma gondii. The primers designed based on a specific conservative target sequence of the 529 gene of the toxoplasma gondii for qualitatively detecting the 529 gene of the toxoplasma gondii in tissues, feces or blood samples comprise an upstream primer and a downstream primer. According to the present invention, a real-time fluorescent RAA technology is used to establish the method for rapid detection of the toxoplasma gondii. Compared with fluorescent quantitative PCR, the method has the advantages of low cost, simpleness and fastness, can conduct detection at constant temperature of 36 DEG C within 20min, and directly read detection results by a portable instrument. The method of the present invention achieves minimum detection size for toxoplasma gondii genomes up to 102 copies, has sensitivity comparable to the traditional fluorescent quantitative PCR, and is suitable for rapid diagnosis of clinical samples and laboratories.
Owner:INST OF ANIMAL SCI OF CHINESE ACAD OF AGRI SCI

Isothermal amplification primer group capable of rapidly detecting cattle and sheep akabane disease viruses and application thereof

The invention discloses an isothermal amplification primer group capable of rapidly detecting cattle and sheep akabane disease viruses and application thereof. Nucleotide sequences of the isothermal amplification primer group are respectively shown as SEQIDNo.1-4. According to the invention, cDNA obtained through reverse transcription on RNA (ribonucleic acid) of a sample is taken as a template, the isothermal amplification primer is utilized for carrying out loop-mediated isothermal amplification detection, results can be judged in the following two ways after reaction is finished: electrophoresis is carried out on amplification products, and the sample with a specific stair-step strip is judged to be positive; calcein is added into a reaction system, judging is carried out by virtue of naked eyes, and the sample with change in colour is judged to carry positive cattle and sheep akabane disease viruses. The isothermal amplification method for detecting cattle and sheep akabane disease viruses by utilizing the isothermal amplification primer is low in requirement on instrument and equipment, rapid, safe, good in specificity and strong in sensitivity, provides a technical support for cattle and sheep akabane disease detection in the animal husbandry, especially rapid detection on cattle and sheep in a basic quarantine department, and has good popularization and application value.
Owner:INSPECTION & QUARANTINE TECH CENT OF GUANGDONG ENTRY EXIT INSPECTION & QUARANTINE BUREAU

A kind of circular isothermal amplification primer for rapid detection of citrus hemipuncture nematode and its application

The invention discloses a loop isothermal amplification primer for quickly detecting tylenchulus semipenetrans and application of the loop isothermal amplification primer. The loop isothermal amplification primer comprises a primer pair TSF3 / TSB3 and a primer pair TSFIP / TSBIP, and the sequences of the primer pairs are shown as SEQ ID NO. 1 to 4 respectively. A loop isothermal amplification method is established through the loop isothermal amplification primer, loop isothermal amplification is performed through taking a sample DNA as a template, and results can be judged in two ways after the end of reaction, wherein the first way is that an amplification primer is subjected to electrophoresis, and a sample of a specific ladder-shaped strip, which occurs, is judged to be positive; the second way is that through adding SYBR green I into a reaction system, a sample of which the color is changed is observed with naked eyes to be positive. The loop isothermal amplification method is low in requirement for instruments and equipment, quick, safe, and high in specificity and sensitivity; a technical support is provided for the detection of the tylenchulus semipenetrans, in particular to the quick detection work of a grass-root quarantine unit for the tylenchulus semipenetrans, and the popularization and application values are very high.
Owner:SOUTH CHINA AGRI UNIV

Loop-mediated isothermal amplification primer set for identifying three kinds of pratylenchus pratensis on sugarcane and kit comprising loop-mediated isothermal amplification primer set

The invention discloses a loop-mediated isothermal amplification primer set for identifying three kinds of pratylenchus pratensis on sugarcane and a kit comprising the loop-mediated isothermal amplification primer set. The loop-mediated isothermal amplification primer set comprises three groups of primers, namely, an outer primer pair PZF3/PZB3 and an inner primer pair PZFIP/PZBIP, an outer primer pair PPF3/PPB3 and an inner primer pair PPFIP/PPBIP, as well as an outer primer pair PBF3/PBB3 and an inner primer pair PBFIP/PBBIP, wherein the nucleotide sequences of the primers are respectively shown as SEQ ID NO.1-12. The three kinds of pratylenchus pratensis are pratylenchus zeae, P. parazeae and P. brachyurus. The loop-mediated isothermal amplification primer set and the kit comprising the loop-mediated isothermal amplification primer set have low requirements on instrument and equipment, are simple, rapid and safe, and are good in specificity and high in sensitivity, and a technical support is provided for the detection for pratylenchus zeae, P. parazeae and P. brachyurus, especially, the rapid identification and distinguishing for the three kinds of pratylenchus pratensis of the grassroots units.
Owner:SOUTH CHINA AGRI UNIV

Ring isothermal amplification primers capable of fast detecting pratylenchus neglectus and application thereof

The invention discloses a ring isothermal amplification primer group capable of fast detecting pratylenchus neglectus. The primer group comprises an outer side primer pair pnF32 / pnB32 and an inner side primer pair of pnFIP2 / pnBIP2. The sequences of primers are shown as the SEQ ID NO.5-8. A ring isothermal amplification method is established according to the primer group, ring isothermal amplification is performed with sample DNA as a template, a result can be adjudged in two modes after reaction ends, according to one mode, electrophoresis is performed on amplification products, and samples with a specific ladder-like strip are considered as positive, and according to the other mode, SYBR green I is added into a reaction system, and samples where color changes are observed through naked eyes are considered as positive. The ring isothermal amplification method is low in requirement for instruments and equipment, fast, safe, good in specificity and high in sensitivity, the method provides technical support for detection of pratylenchus neglectus, particularly, a basic layer quarantine unit provides technical support for fast detection work of pratylenchus neglectus, and good application and popularization value is achieved.
Owner:林康艺

A set of loop-mediated isothermal amplification primers and their kits for the identification of three species of Brachybody nematodes on sugarcane

The invention discloses a loop-mediated isothermal amplification primer set for identifying three kinds of pratylenchus pratensis on sugarcane and a kit comprising the loop-mediated isothermal amplification primer set. The loop-mediated isothermal amplification primer set comprises three groups of primers, namely, an outer primer pair PZF3 / PZB3 and an inner primer pair PZFIP / PZBIP, an outer primer pair PPF3 / PPB3 and an inner primer pair PPFIP / PPBIP, as well as an outer primer pair PBF3 / PBB3 and an inner primer pair PBFIP / PBBIP, wherein the nucleotide sequences of the primers are respectively shown as SEQ ID NO.1-12. The three kinds of pratylenchus pratensis are pratylenchus zeae, P. parazeae and P. brachyurus. The loop-mediated isothermal amplification primer set and the kit comprising the loop-mediated isothermal amplification primer set have low requirements on instrument and equipment, are simple, rapid and safe, and are good in specificity and high in sensitivity, and a technical support is provided for the detection for pratylenchus zeae, P. parazeae and P. brachyurus, especially, the rapid identification and distinguishing for the three kinds of pratylenchus pratensis of the grassroots units.
Owner:SOUTH CHINA AGRI UNIV

A set of isothermal amplification primers for rapid detection of bovine and sheep Akabane disease virus and its application

The invention discloses a group of isothermal amplification primers for rapid detection of cattle and sheep Akabane disease virus and application thereof. The nucleotide sequences of the primers are respectively as SEQ? ID? Shown in NO.1~4. In the present invention, the cDNA obtained by sample RNA reverse transcription is used as a template, and the above-mentioned primers are used for loop-mediated isothermal amplification detection. After the reaction, the result can be judged in two ways: one is that the amplified product is subjected to electrophoresis, and a specific ladder-like appearance occurs. The sample of the strip is judged as positive; the second is by adding calcein to the reaction system, and judged by naked eyes, the sample with color change is judged as positive for bovine and sheep Akabane disease virus. The isothermal amplification method for detecting Akabane disease virus in cattle and sheep by using the primers in the present invention has low requirements on instruments and equipment, is fast, safe, has good specificity, and has strong sensitivity. The quarantine unit has provided technical support for the rapid detection of cattle and sheep, which has very good promotion and application value.
Owner:INSPECTION & QUARANTINE TECH CENT OF GUANGDONG ENTRY EXIT INSPECTION & QUARANTINE BUREAU
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