30results about How to "No amplification" patented technology

The invention relates to a kit for rapidly detecting pathogeny of acute hepatopancreatic necrosis disease of prawns and application of the kit, belonging to technical field of biotechnology. The kit comprises an LAMP primer group, DNA polymerase, LAMP reaction liquid, a positive control and a negative control. The kit further comprises a color developing agent. The LAMP primer group comprises a pair of outer primers, a pair of inner primers and a pair of loop primers. The application of the kit in the pathogeny detection of the acute hepatopancreatic necrosis disease of the prawns comprises the steps of purifying and separating vibrio strains, preparing vibrio DNA, carrying out constant temperature gene amplification reaction, and carrying out result judgment by virtue of a turbidity meter or an ESE-Quant Tube Scanner. The kit has the advantages of good specificity, high sensitivity, simple operation, reliable result and the like, and is applicable to the rapid detection of prawn farming sites.

The invention dislcoses an RAA (recombinase-aid amplification) constant-temperature fluorescence detection method and a detection kit for EHP (enterocytozoon hepatopenaei). The detection kit comprisesa forward primer SEQ ID NO. 1, a reverse primer SEQ ID NO. 2, a specific fluorescence probe SEQ ID NO. 3, reaction liquid, recombinant polymerase and a reference substance. The kit has the advantagesthat the specificity is strong; the detection sensitivity is high, and can reach 100fg/mu L; high accuracy and reliability are achieved; the operation is simple and rapid, and the kit is suitable forfield detection and has wide application scenarios.

The invention discloses primers and a probe for rapidly and quantitatively detecting duck adenovirus type 4 and a detection method and application of the primers and the probe. The sequences of the primers are as shown in SEQ ID NO.1-2, and the sequence of the probe is as shown in SEQ ID NO.3. The fluorescent PCR method capable of rapidly and quantitatively detecting the duck adenovirus type 4 inthe clinical sample is established for the first time; the detection method is simple to operate, the whole operation process does not exceed 3 hours, the sensitivity is high, the specificity is good,the repeatability is good, quantitative analysis can be accurately and rapidly carried out with high flux, and the detection method is beneficial to popularization and application in clinical practice.

The invention relates to the field of animal disease molecular biology detection methods and detection agents, in particular to an animal Torque Teno virus rapid detection primer, a kit and a detection method using a loop-mediated isothermal amplification (LAMP) technology. Multiple comparisons are carried out by using Clustal W according to two different serotype gene sequences of an animal Torque Teno virus, and conserved zones of the sequences are analyzed, an inner primer and an outer primer are respectively designed by adopting LAMP primer design software, and detection and identification of TTV1 and TTV2 serotypes are realized rapidly specifically. The animal Torque Teno virus detection method disclosed by the invention has the advantages of rapidness, high sensitivity, strong specificity, convenience for operation, low requirement of equipment, time and labor saving, easiness in observing results, no complex post-treatment, and wide application range.

The invention relates to the technical field of gene engineering, in particular to a molecular marker for identifying tremella aurantialba and an application of the molecular marker, a primer pair ishigh in specificity, tremella aurantialba DNA derived from tremella aurantialba can be subjected to specific amplification, 635bp fragments can be amplified, and no amplification effect on other localtremella aurantialba strains exists. The molecular markers, probes and/or kits for the tremella aurantialba can be specifically designed by utilizing the primer pair, the tremella aurantialba is screened and identified, tremella aurantialba strains from the tremella aurantialba can be simply, conveniently, quickly and accurately screened by utilizing the method, and the method has important significance for genetic research and market popularization of the tremella aurantialba strains.

The invention discloses a recombinase-aid amplification (RAA) thermostatic fluorescence detection method of infectious hypodermal and hematopoietic necrosis virus (IHHNV) of prawns, and a detection kit. The detection kit comprises a forward primer shown in SEQ ID No. 1, a reverse primer shown in SEQ ID No. 2, a specific fluorescent probe shown in SEQ ID No. 3, a reaction solution, recombinant polymerase and a reference substance. The kit provided by the invention is high in specificity; the detection sensitivity is high, and can reach up to 0.32fg/mu L; the detection method has the advantagesof high accuracy, reliability, simple, convenient and fast operation, and suitability for field detection, thus having wide application prospect.

The invention discloses an LAMP detection primer group for Siniperca chuatsi-perch rhabdovirus, application of the LAMP detection primer group and a detection kit. The primer group comprises a pair ofouter primers, a pair of inner primers and a pair of loop primers; the outer primers comprise a sequence L-F3 and a sequence L-B3, the sequence L-F3 of the outer primers is shown in SEQ ID NO: 1, andthe sequence L-B3 of the outer primers is shown in SEQ ID NO: 2; the inner primers comprise a sequence L-FIP and a sequence L-BIP, the sequence L-FIP of the inner primers is shown in SEQ ID NO: 3, and the sequence L-BIP of the inner primers is shown in SEQ ID NO: 4; and the loop primers comprise a sequence L-LF and a sequence L-LB, the sequence L-LF of the loop primers is shown in SEQ ID NO: 5, and the sequence L-LB of the loop primers is shown in SEQ ID NO: 6. The invention further provides application of the primer group in preparation of a Siniperca chuatsi-perch rhabdovirus detection kitand the kit. The primer group and kit, provided by the invention, have the advantages of simplicity in operation, high detection speed, good specificity, high sensitivity, reliable result, and the like.

The invention discloses an LAMP (loop-mediated isothermal amplification) detection primer group, a kit and a detection method for letalurus punetaus herpesviruses and belongs to the field of disease prevention and control in aquaculture. The kit consists of an LAMP primer group, DNA (deoxyribonucleic acid) polymerase, an LAMP reaction liquid, positive control, negative control and a developing agent, wherein the LAMP primer group comprises a pair of outer primers, a pair of inner primers and a pair of loop primers. The detection kit comprises the following application steps in detection on theletalurus punetaus herpesviruses: preparing DNA of the letalurus punetaus herpesviruses, performing a constant-temperature gene amplification reaction and performing result judgment by using a real-time fluorescence quantitative PCR (polymerase chain reaction) instrument. The kit disclosed by the invention has the advantages of being simple to operate, rapid in detection, good in specificity, high in sensitivity, reliable in result, and the like, can play roles in early-stage rapid diagnosis and real-time monitoring on channel catfish virus diseases, and is applicable to rapid detection on pathogens on a letalurus punetaus breeding site.

The invention discloses a fast detection primer, reagent kit and method for channel catfish viruses and an application of the fast detection primer, the reagent kit and the method, and belongs to thefield of a biological technology. The method comprises steps of designing a PCR primer and a probe, preparing a DNA template, performing PCR amplification and performing result judging through luminescence signals. In accordance with gene conserved sequences corresponding to the channel catfish viruses, the primer and a taqMan probe are designed, and through sufficient optimization, the primer probe and the reaction condition are originally created, so that the method for quickly and reliably detecting the channel catfish viruses through fluorescent quantitation PCR is established. According to the fast detection primer, reagent kit and method, quantification of the DNA template is realized, and the fast detection primer, the reagent kit and the method have the advantages of being simple to operate, quick to detect, good in specificity, high in sensitivity, reliable in results and the like, and can exert important effects in respects of early rapid diagnosis and real-time monitoring ofthe channel catfish viruses.