首页> 外国专利> KIT FOR DNA DETECTION OF BOVINE IMMUNODEFICIENCY PROVIRUS CONTAINING A PAIR OF SPECIFIC PRIMERS AND PROBE AND DIAGNOSTIC TECHNIQUE FOR CATTLE IMMUNODEFICIENCY VIRUS BY POLYMERASE CHAIN REACTION IN REAL TIME

KIT FOR DNA DETECTION OF BOVINE IMMUNODEFICIENCY PROVIRUS CONTAINING A PAIR OF SPECIFIC PRIMERS AND PROBE AND DIAGNOSTIC TECHNIQUE FOR CATTLE IMMUNODEFICIENCY VIRUS BY POLYMERASE CHAIN REACTION IN REAL TIME

机译:聚合酶链反应实时检测牛特异性免疫缺陷牛血清的试剂盒和牛免疫缺陷病毒的诊断技术

摘要

FIELD: biochemistry.;SUBSTANCE: invention relates to biochemistry. Described is kit for DNA detection of bovine immunodeficiency provirus (BIV (bovine immunodeficiency virus)), containing pair of specific primers and DNA-probe, by PCR in real time. Primers and probe have following nucleotide composition (5′-3′-): pf - TAGGGTAGTGGGATCTCAGAAATC, pr - ACATCCGTAACATCTCCTACCATC, z - GAGGATGGTAGGAGATGTTACGGAT. Source of fluorescence at 5′ end of the probe used is dye ROX and fluorescence quenching fluorescence on 3′ end of BHQ2. Also described is diagnostic technique for BIV by PCR in real time using kit according to claim. 1. Reaction mixture is prepared by mixing buffer 10-fold for PCR - 2.5 mql, dNTP (25 mM) is 0.2 mql, pf and pr primers (10 pmol/mql) by 1 mql, probe z (10 pmol/mql) is 0.5 mql, Taq polymerase (5 units/mql) is 0.2 mql, MgCl2 (50 mM) is 2 mql, bidistilled water is 7.6 mql, and amplification is carried out as follows: denaturation 95°C is 5 minutes, cycling: denaturation (95°C - 20 s) - annealing (55°C - 20 s) - elongation (72 C - 20 s), wherein cycle of denaturation-annealing-elongation is repeated 10 times, cycling 2 with detection: denaturation (95°C - 20 s)-annealing (55°C - 20 s)-elongation (72°C - 20 s), wherein cycle denaturation-annealing-elongation is repeated 25 or 30 times. Fluorescence is measured over a Orange channel at temperature of 55°C. Intersection of fluorescence curve line threshold, set at level of 30% of maximum level of fluorescence in last cycle amplification testifies to provirus BIV presence in sample, at that, the less value of “Ct” indicator, the higher amount of provirus BIV in analysed sample, while absence of intersection of fluorescence curve line threshold testifies to absence of provirus BIV in sample.;EFFECT: invention can be used in scientific research for detecting genetic material BIV in animal blood lymphocytes by PCR in real time.;2 cl, 6 dwg, 3 tbl, 2 ex
机译:技术领域本发明涉及生物化学。所描述的是通过实时PCR通过DNA检测牛免疫缺陷原病毒(BIV(牛免疫缺陷病毒))的试剂盒,其包含一对特异性引物和DNA探针。引物和探针具有以下核苷酸组成(5'-3'-):pf-TAGGGTAGTGGGATCTCAGAAATC,pr-ACATCCGTAACATCTCCTACCATC,z-GAGGATGGTAGGAGATGTTACGGAT。所用探针5'端的荧光源是染料ROX和BHQ2 3'端的荧光猝灭荧光。还描述了使用根据权利要求的试剂盒通过PCR实时诊断BIV的技术。 1.通过混合10倍用于PCR的缓冲液制备反应混合物-2.5 mql,dNTP(25 mM)为0.2 mql,pf和pr引物(10 pmol / mql)乘以1 mql,探针z(10 pmol / mql)为0.5 mql,Taq聚合酶(5单位/ mql)为0.2 mql,MgCl 2 (50 mM)为2 mql,双蒸馏水为7.6 mql,扩增过程如下:变性95°C 5分钟,循环:变性(95°C-20 s)-退火(55°C-20 s)-延伸(72 C-20 s),其中变性-退火-延伸的循环重复10次,循环2带有检测:变性(95℃-20s)-退火(55℃-20s)-伸长(72℃-20s),其中循环变性-退火-伸长重复25或30次。在温度为55°C的橙色通道上测量荧光。荧光曲线线阈值的交点,设置为最后循环扩增中最大荧光水平的30%,证明样品中存在原病毒BIV,因此,“ Ct”指标值越小,分析的原病毒BIV含量越高样本;而没有荧光曲线线阈值的交集则证明样本中不存在原病毒BIV 。;效果:本发明可用于科学研究,通过PCR实时检测动物血淋巴细胞中的遗传物质BIV。2cl,6 dwg,3汤匙,2前

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