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1.
近交系大鼠DNA指纹图稳定性的研究   总被引:1,自引:0,他引:1  
为建立DNA指纹技术在近交系大鼠遗传监测中的方法,采用DNA指纹图对国内已知的7个品系近交系大鼠群体进行了分析,并对相同DNA进行了多次DNA指纹图重复实验,其结果表明:不同品系之间DNA指纹图差异较大,其平均图带数为(16.360±2.178),共有带率为(0.061±0.008),相似系数为(0.062±0.008),相同DNA指纹图概率为3.691×10-23。相同DNA不同次制作的DNA指纹图谱基本一致(P>0.05)。同一个体不同组织的DNA指纹图也基本相同,从而证实了该方法具有高度的稳定性和可重复性。  相似文献   

2.
两个家系猪的DNA指纹图谱遗传分析   总被引:3,自引:1,他引:2  
本文用人源小卫星探针33.6和33.15获得了两个家系猪的DNA指纹图谱。通过对F1和F2代家系分析,证实DNA指纹图带以孟德尔方式遗传。在家系2(探针33.6)的1个后代中发现了一条新突变带。文中还对这两个探针检测到的位点数进行了估测  相似文献   

3.
用鸡的8个小卫星探针进行鸡的DNA指纹分析   总被引:4,自引:0,他引:4  
本研究用克隆的8个鸡的小卫星探针(cMS7、cMS13B、cMS13S、cMS14、cMS18、cMS20、cMS21、cMS28)对4 ̄5只鸡进行了DNA指纹分析。结果表明,它们都能产生具有高度变异性的DNA指纹图,平均带数为25.3 ̄37.8,平均相似系数为0.257 ̄0.409。用鸡的小卫星探针cMS18、cMS20、cMS21、cMS28及人源小卫星33.15与同一张印迹膜的杂交分析表明,  相似文献   

4.
用EDS76病毒标准AV127株和分离株(B96株)感染鸭胚,提取病毒核酸,分别经EcoRl和Pstl双酶切,获得图形和大小相似的酶切片段。分别进行EcoRl和Pstl单酶切,也得到相似结果。病毒DNA经EcoRl和Pstl双酶切后,与PUC19质粒载体重组,并转化到EcoliJM101中,筛选出一个插入片段(G片段)约为27kb的重组质粒。用Digoxigemin标记EDS76DNAG片段(EcoRl和Pstl双酶切片段)及含该片段的重组质粒分别制备探针,对EDS76病毒DNA进行斑点杂交,两种探针均为阳性,而对照组NDV、IBV、ILTV、IBDV正常鸭胚尿囊液的核酸为阴性。且后一种探针的敏感性高于前者,它的DNA检出限量为4pg水平。结果表明,两种探针具有高度的特异性、敏感性。  相似文献   

5.
用DHBV阳性血清经腹爱感染雏鸭后,药物试验组与对照组DHBV感染率分别为67.61%、67.61%、65.52%。经复方乙肝解毒丸治疗2个月后,采集血清作DHBV-DNA斑点杂交试验,结果,药物试验组与对照组转阴率分别为34.04%,7.89%。两组有显著差异。鸭乙肝病毒与人乙肝病毒同属嗜肝DNA病毒,本实验结果为临床治疗乙肝患者提供了可靠依据。  相似文献   

6.
DIG—标记鸡传染性法氏囊病病毒cDNA探针的制备   总被引:7,自引:1,他引:6  
用IBDV特异引物对IBDV RNA进行逆转录和PCR扩增。以低融点琼脂糖凝胶电泳法回收PCR扩增带,经酚-氯仿纯化后,用DIG标记制备IBDV cDNA核酸探针。斑点杂交试验证明,该探针能与IBDV不同毒株发生阳性杂交反应,敏感度为1pg。本实验制备的IBDV cDNA核酸探针不仅为IBDV的流行病学研究和分子生物学鉴定提供了敏感可靠的手段,而且也是核酸探针制备方法的一次探索。  相似文献   

7.
用DHBV阳性血清经腹腔感染雏鸭后,药物试验组与对照组DHBV感染率分别为67.61%、65.52%。经复方乙肝解毒丸治疗2个月后,采集血清作DHBV-DNA斑点杂交试验。结果,药物试验组与对照组转阴率分别为34.04%、7.89%。两组有显著差异。鸭乙肝病毒与人乙肝病毒同属嗜肝DNA病毒,本实验结果为临床治疗乙肝患者提供了可靠依据。  相似文献   

8.
用IBDV特异引物对IBDVRNA进行逆转录和PCR扩增。以低触点琼脂糖凝胶电泳法回收PCR扩增带,经酚-氯仿纯化后,用DIG际记制备IBDVCDNA核酸探针.斑点杂交试验证明,该探针能与IBDV不同毒株(STC、Lukert、B_2和LQ)发生阳性杂交反应,敏感度为1pg.本实验制备的IBDVcDNA核酸探针不仅为IBDV的流行病学研究和分子生物学鉴定提供了敏感可靠的手段,而且也是核酸探针制备方法的一次探索。  相似文献   

9.
减蛋综合征病毒基因组DNA的酶切分析   总被引:3,自引:0,他引:3  
采用差速离心法化了鸭胚尿囊液中的减蛋综合征(EDS-76)病毒WPDV205株并提取了病毒基因组核酸。选用EcoRI和BamHI两种限制性内切酶分别对病毒基因组DNA刊物单酶切和双酶切处理,单酶切消化均产生4个片段、双酶切消化产生7个惩段。用琼脂糖凝胶电泳方法测定了病毒基因组DNA和所有酶切片段的分子质量,将这些结果与AV-127标准株和B8-78株基因组DNA由相贩内切酶消化的结果进行比较,发现  相似文献   

10.
用核酸探针检测新城疫病毒的研究   总被引:1,自引:0,他引:1  
用光敏生物素标记鸡新城疫cDNA制备核酸探针,经斑点杂交和碱性磷酸酶显色后,探针同该cDNA的PCR产物,PCR产物重组子和新城疫强,弱毒株呈现阳性反应,与IBV,ILT,MG和正常尿囊液等均呈阴性杂交反应,田间病料的杂交试验也表明该cDNA探针是且特异的检测方法。  相似文献   

11.
用连续线性梯度聚丙烯酰胺凝胶电泳技术分离北京鸭血浆蛋白,在后转铁蛋白区Potf2发现了由2个等位基因构成的3种基因型利用Potf2的基因频率计算了现有北京鸭育成品率间的遗传距离并进行了聚类分析,北北京鸭的6个品系分成两类,这两类愉 好分别作杂交配套的父本和母本,其中父系的Potf2A基因的频率显著高于母系,分别统计北京鸭6个品系和3种基因型的49日龄体重并进行了多重比较,发现品系的平均体重越大等位  相似文献   

12.
Sequences of papillomavirus DNA in equine sarcoids   总被引:2,自引:0,他引:2  
DNA was extracted from 14 equine sarcoids, electrophoresed and hybridised with a radioactively labelled probe of bovine papillomavirus type I (BPV 1) DNA under conditions of low stringency. Twelve sarcoids contained sequences of DNA that hybridised with the probe and that comigrated with BPV 2 DNA. The viral DNAs in four of these sarcoids differed from BPV 1 and BPV 2 DNA on restriction endonuclease analysis. One of four cell lines derived from sarcoids also contained BPV 1 related DNA. The results confirm the frequent presence in equine sarcoids of unintegrated papillomaviral DNA and suggest a role for papillomavirus infection in this disease.  相似文献   

13.
The DNA isolated from cow-hamster hybrid somatic cells segregating bovine chromosomes was analyzed by Southern blotting and hybridization with a heterologous [32P]-labeled porcine cDNA probe encoding insulin-like growth factor I (IGF-I). Thirteen of 25 cow-hamster hybrid cell lines exhibited the bovine-specific IGF-I fragment. Analysis for the retention or loss of bovine IGF-I with markers previously screened against the same panel of hybrid cells revealed a 100% concordance with lactate dehydrogenase B of bovine syntenic group U3 located on bovine chromosome 5. Restriction fragment length analyses of genomic DNA from animals representing five breeds (Angus, Polled Hereford, Simmental, Gelbvieh, and Belgian Blue) and from seven half-sib Angus calves indicated that polymorphisms for the genomic composition of the bovine IGF-I gene may exist in cattle populations.  相似文献   

14.
0~3周龄北京鸭氨基酸理想模式的研究   总被引:5,自引:1,他引:5  
依据扣除法原理,根据现有氨基酸需要量标准和目前的研究结果规划出一种氨基酸模式,依次将模式中赖氨酸、蛋氨酸、色氨酸、苏氨酸、异亮氨酸扣除20%,而非扣除的氨基酸量保持不变,来确定扣除某一种氨基酸后对育雏期北京鸭生产性能和血液生化指标的影响,确定出理想的氨基酸比例。试验共设6个处理组,为6种氨基酸模式,每个处理设4个重复。结果表明:北京鸭育雏期氨基酸理想模式为赖氨酸:蛋氨酸:色氨酸:苏氨酸:异亮氨酸=100:42:22:38:48。  相似文献   

15.
By using a defined cDNA probe for the VH region of a murine phosphocholine-binding myeloma protein (S107) we have defined a family of distinct cross-hybridizing DNA sequences in genomic DNA of the goldfish. The estimated number of the goldfish putative VH family detectable by the S107 probe is about 36. By using two putative goldfish VH probes to analyze, by hybridization, the relationships among seven of the goldfish genomic clones, we have determined that the putative goldfish VH genes recognized by the S107 probe comprise at least several distinct families that are not closely related.  相似文献   

16.
A genomic library was prepared from Brucella suis DNA (MboI digested) and cloned into the BamHI site of pUC18. Colony hybridisation using a probe prepared from purified B. suis DNA labelled with alpha 32P was carried out to identify colonies of interest. About 20 colonies, which gave an intense signal upon hybridisation with whole B. suis genomic DNA as a probe, were selected. Because of the high degree of DNA homology between B. suis and Brucella abortus, a short probe was chosen as it would more likely give species specificity. Of seven fragments selected to probe whole B. suis, B. abortus, and Yersinia enterocolitica DNA, one was found to hybridise with B. suis only. The probe was sequenced in two directions and sense and anti sense primers of 25bp in length were chosen to yield a product of 421bp. After optimisation of the PCR, a product of 420bp was obtained with B. suis template DNA and two bands of 420 and 650bp were detected with B. abortus template DNA. This is the first reported PCR of the Brucella genome where a single pair of primers will discriminate between B. suis and B. abortus. No band was observed when the two primers were used to amplify E. coli, Y. enterocolitica, Enterobacter cloacae, Staphylococcus aureus, Streptococcus uberis, Corynebacterium bovis, or Serratia marcescens template DNA.  相似文献   

17.
A panel of three DNA probes were derived at random from a genomic DNA library of Campylobacter mucosalis strain E8384-4. Each probe hybridized specifically to C. mucosalis DNA from bacteria fixed to nylon membranes. The probes did not hybridize to DNA from other Campylobacter species or to other bacteria even at 100-fold higher amounts. Each probe hybridized to all of 24 isolates of C. mucosalis which had been collected over time from different geographic locations. Southern blot analysis of selected C. mucosalis isolates was carried out to determine if the probes would be useful for differentiating among various isolates. It indicated that restriction fragment length polymorphisms (RFLPs) exist at the loci identified by our probes. These differences were used to characterize seven C. mucosalis isolates recovered from pigs in Minnesota. The results suggest that RFLP analysis may be a useful tool for epidemiological studies of C. mucosalis.  相似文献   

18.
采用单因子完全随机试验设计研究饲粮维生素D水平对120日龄雌性龙岩麻鸭产蛋性能,血液生化及胫骨指标的影响,进而探讨产蛋初期蛋鸭维生素D需要量。选取1 260只120日龄健康的福建龙岩麻鸭随机分为6个处理,每处理6个重复,每重复35只。各处理组蛋鸭随机饲喂维生素D水平分别为0、800、1 600、2 400、3 200、4 000 IU/kg的试验饲粮。饲养期为21 d。结果表明:维生素D水平对产蛋初期龙岩麻鸭产蛋性能、蛋品质以及血浆钙、磷含量、碱性磷酸酶活性均无显著影响(P>0.05),基础饲料上添加维生素D显著降低血浆中甲状旁腺激素的含量(P<0.05),但各添加组间无显著差异(P>0.05),饲粮维生素D含量显著影响胫骨钙、磷及灰分含量(P<0.05),维生素D水平为800 IU/kg时,获得较好的骨骼质量,维生素D水平对胫骨长度、胫骨管围、折断力、骨密度、骨矿物盐含量无显著影响(P>0.05)。因此,龙岩麻鸭产蛋初期饲粮维生素D适宜添加量为800 IU/kg。  相似文献   

19.
本试验用DNA池法从40条随机引物中筛选出29条多态性、重复性好的引物,对贵州黄鸡、兴黔黄鸡、乌骨鸡三个培育品种(系)和地方品种兴义矮脚鸡及引进选育品种矮脚黄鸡共五个品种(系)进行随机扩增多态亲缘关系分析。结果表明,29条引物共扩增出稳定、清晰、重复性好的条带190条,其中多态性片段127条,在300bp ̄3000bp之间。单个引物扩增出的RAPD条带在4 ̄13条之间,平均为6.55条。五个品种(系)间的亲缘关系符合它们的育种背景[1,2,3]。  相似文献   

20.
根据GPV H1株核苷酸序列,设计了扩增VP1-VP3基因非重叠序列的1对引物,对其结构蛋白VP1与VP3非重叠核苷酸序列进行PCR扩增,将PCR产物纯化、回收后制备出GPV VP1-VP3基因DIG标记核酸探针,其标记效率达到0.1pg/μl。特异性检测结果表明,该探针能与GPV不同毒株核酸发生特异性杂交,而与对照的DPV、GPMV等病毒的核酸杂交反应均为阴性;敏感性检测结果表明该探针对GPV的最低检出量为0.032ng。上述试验结果表明该探针可以用于GPV感染临床病料的检测。  相似文献   

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