首页> 外国专利> METHOD OF SIMULTANEOUS GENODIAGNOSTIC OF TWO MUTANT ALLELES CAUSING CVM AND BLAD IN CATTLE, AND TEST SYSTEM FOR IT

METHOD OF SIMULTANEOUS GENODIAGNOSTIC OF TWO MUTANT ALLELES CAUSING CVM AND BLAD IN CATTLE, AND TEST SYSTEM FOR IT

机译:牛中CVM和叶片突变的两个突变等位基因的同时遗传学检测方法及其测试系统

摘要

FIELD: biotechnologies.;SUBSTANCE: series of inventions relates to biotechnology. Method of simultaneous genodiagnostic of two mutant alleles, causing CVM and BLAD in cattle, involves DNA recovery from biological material polymerase chain reaction in real time using the reaction mixture (test system) with CVM/BLAD, containing 50 mMKCl, 50 mMTRIS-HCl, 250 nMdNTP, 2.5 mMMgCl2, primers - in the concentration of 200 nm, allele-specific probes in concentration of 100 Nm, having the following sequence: CVM_up - gattctcaagagcttaattctaagga, CVM_low - aagtaaaccccagcaaagccac, CVM_Wt - (FAM) aggtctcatggcagttct-(BHQ1), CVM_m - (R6G) catggcatttctcacagcat-(BHQ2), BLAD_up - ttaggcagttgcgttc, BLAD_low - acgttgacgaggtcatccacca, BLAD_Wt - (ROX) accccatcgacctgtacta-(BHQ1), BLAD_m (Cy5) ccatcggcctgtactacct-(BHQ2), diluent, 2.5 units. Taq DNA polymerase, three positive and one negative control sample. During preparation for conducting reaction required volume of components is calculated, based on the number of analyzed samples plus 4, reagents are mixed, then 20 mcl of the prepared PCR mixtures are added to test tubes prepared for PCR, 5 mcl of the control and analyzed samples are added into each PCR test tube, test tubes are placed into amplifier, primers annealing takes place at the stage of cycling at 64 °C for 30 s at number of cycles amplification equal to 40. Derived data is carried out by comparing the amplified genome sections, results are interpreted based on the presence or absence of intersection of fluorescence curve with threshold line installed at appropriate level.;EFFECT: invention enables diagnosing two mutant alleles simultaneously, causing CVM and BLAD in cattle, reduces time for RT PCR performing.;2 cl, 3 dwg, 4 tbl
机译:领域:生物技术。系列发明涉及生物技术。同时引起牛牛CVM和BLAD突变的两个等位基因的基因诊断方法包括使用含有50 mMKCl,50 mMTRIS-HCl,CVM / BLAD的反应混合物(测试系统)实时从生物材料聚合酶链反应中回收DNA。 250 nMdNTP,2.5 mMMgCl 2 ,引物-浓度为200 nm,等位基因特异性探针的浓度为100 Nm,具有以下序列:CVM_up-gattctcaagagcttaattctaagga,CVM_low-aagtaaaccccagcaaagccac,CVM_Wt-(FAM )aggtctcatggcagttct-(BHQ1),CVM_m-(R6G)catggcatttctcacagcat-(BHQ2),BLAD_up-ttaggcagttgcgttc,BLAD_low-acgttgacgaggggcatccacca,BLAD_Wtt-(ROX)-actc,QtC(2)单位。 Taq DNA聚合酶,三个阳性和一个阴性对照样品。在准备进行反应的过程中,根据分析样品的数量加4,计算所需的组分体积,然后混合试剂,然后将20 ml的制备好的PCR混合物添加到准备用于PCR的试管中,将5 ml的对照加入并分析将样品添加到每个PCR试管中,将试管放入放大器中,引物退火在64°C循环30 s的阶段进行,扩增的循环数等于40。通过比较扩增后的数据来获得数据基因组部分,基于荧光曲线与在适当水平上安装的阈值线的相交的存在与否来解释结果。效果:本发明能够同时诊断两个突变等位基因,从而在牛中引起CVM和BLAD,减少了进行RT PCR的时间。 ; 2 cl,3 dwg,4 tbl

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