荧光标记复合扩增检测4个STR基因座多态性

目的建立荧光标记复合扩增D1S2142,D13S1492,D14S306,D15S659基因座检测分型方法,并对成都汉族群体4个基因座的遗传多态性进行调查。方法用6-FAM标记D1S2142和D15S659引物,HEX、TMR分别标记D14S306和D13S1492引物,PCR复合扩增,310基因分析仪电泳自动收集电泳结果数据,GeneScan Analysis Software3.7NT软件计算扩增产物片段相对大小,Genotyper(3.7NT软件进行样本基因型分型,建立了荧光标记复合扩增检测4个STR基因座基因型的方法,对145名成都汉族无关个体样本进行分型。结果荧光标记复合扩增D1S2142,D13S1492,D14S306,D15S659基因座,每个STR基因座都获得了清晰的基因型分型结果。145份样本,4个STR基因座分别检出10,14,7,12个等位基因和22,54,21,39种基因型,其基因型分布均符合Hardy-W e inberg平衡。4个基因座在成都汉族群体的杂合度分别依次为0.7793,0.8345,0.7793和0.8345;多态信息含量分别依次为:0.7656,0.8730,0.7470和0.8312。累计非父排除率为0.9783,累计个人识别机率为0.9999 917。结论荧光标记复合扩增D1S2142,D13S1492,D14S306,D15S659基因座,可实现对每个基因座准确分型;成都汉族群体该4个基因座的遗传学数据,可为群体遗传学和法医学研究与应用提供基础资料。     

Race-Based Peremptory Challenges: An Empirical Analysis of Litigation from the U.S. Court of Appeals, 2002–2006

This paper examines race-based peremptory challenges. Such challenges occur during the voir dire jury selection process. The process allows both the defense and the prosecution to strike jurors who they believe will not decide cases fairly. However, in the case of Batson v. Kentucky 476 U.S. 79 (1986), the Supreme Court ruled that race could not be used as a factor in eliminating prospective jurors. This paper examines federal litigation for five years in which it was alleged that race was used as a factor in removing a juror. An examination of the cases revealed that most of the cases involved sole male litigants who allege that there were multiple race-based peremptory challenges used in their cases. Moreover, most of the cases that led to the allegations involved violent offenses. Other case characteristics are noted, but of most significance was the finding that most appellants lost their cases. As such, the courts felt that most of the challenges were, in fact, race neutral. The implications of this research are discussed. This study was funded by an undergraduate research grant from Penn State University.     

PCR-DGGE法检测浮游生物16S rDNA在溺死鉴定中的应用

目的建立并评估PCR-DGGE法检测浮游生物对溺死鉴定的应用价值。方法大白兔30只随机分为3组:溺死组(n=12),死后抛尸组(n=12)和对照组(n=6);溺死组和死后抛尸组又分为2个亚组:东湖水域组(n=6)和墨水湖水域组(n=6)。死后提取心血和肺、肝、肾、脑等组织,匀浆后,采用Percoll密度梯度离心法分离浮游生物并提取其DNA,PCR扩增浮游生物特异的16S rDNA片段后分别用琼脂糖凝胶电泳及DGGE检测分析。2个溺死案例检材同法检验。结果溺死组各组织器官中浮游生物检测多呈阳性:肺(100%)、肝(83%)、肾(75%)、心血(83%)、脑(42%);死后抛尸组仅2例肺组织(16.7%)检出阳性;对照组全部阴性。溺尸肺组织DGGE分型图谱与相应溺死点水样分型图谱相似,而与非溺死点水样分型结果差异显著。2实际案例均呈阳性。结论本方法不仅有助于定性诊断溺死,而且通过比较产物的多样性可以推断溺死地点,在法医学溺死鉴定中具有较大实用价值。     

Zurechnung des Verkäufers bei Einwendung gegen finanzierenden Leasinggeber

Beim mittelbaren Finanzierungsleasing ist der Vertreter einer Verk?uferfirma (= Lieferantin des Leasinggutes), der auch Vertragsformulare der Leasingfirma mit sich führt, auch Mann ihres Vertrauens im Hinblick auf die richtige übermittlung der Anbot- und Annahmeerkl?rungen den Leasingvertrag betreffend. Zur Gew?hrleistung und dem (Nicht-)Bestehen eines Einwendungsdurchgriffs beim mittelbaren Finanzierungsleasing.     

Two examples of null alleles at the D19S433 locus due to the same 4 bp deletion in the presumptive primer binding site of the AmpFlSTR Identifiler kit

Two cases of allelic loss at the D19S433 locus after multiplex PCR with the AmpFlSTR Identifiler kit (Applied Biosystems) are described. In both cases the failure of PCR resulted in genetic inconsistencies due to opposite homozygosity. After singleplex PCR with published primers additional alleles were observed and Mendelian inheritance was restored. These PCR products were sequenced and in both cases the same 4 bp deletion near the 3′ end of the repeat region was detected in two alleles of different length. The frequency of these null alleles (two events in 1026 allelic transfers) amounts to 0.0019 (95% confidence limits: 0.0002-0.0070).     

一些常见药物在ODS柱上的分离

应用高效液相色谱技术,进行药物的分离、分析已有很多报导。为了在尽可能简便的条件下.较为有效地进行一些药物,主要是弱极性结构药物的初步判断,我们采用 ODS 柱做了些探索。对于一些常见药物,如巴比妥类、安定类、解热镇痛类及某些抗菌素类药物均能观察到较为满意的分离效果。     

我国规模化肉牛场牛病毒性腹泻-粘膜病流行状况监测

从山东、河南和河北省的６个规模化肉牛场随机采肉牛血清８９份，直肠粪拭子１６５份，分别用微量细胞中和试验和双抗体夹心ＥＬＩＳＡ试剂盒检测牛病毒性腹泻粘膜病（ＢＶＤＭＤ）的抗体和抗原。诊断结果：ＢＶＤＭＤ中和抗体阳性率为４６．２％～６５．０％；ＢＶＤＭＤ病毒抗原阳性检出率为５．１％～７７．２％。从而证实我国中原地区肉牛群中存在有ＢＶＤＭＤ。     

狐狸奇异变形杆菌的分离与鉴定

无菌采取病死狐狸内脏,用LB液体培养基和麦康凯琼脂平板培养,分离到1株细菌,通过对该菌的形态特征、培养特性、生化特性进行分析,初步鉴定为变形杆菌。用PCR方法扩增该分离菌株的16 SrRNA基因,结果获得大小为1 539 bp的DNA片段(已登录GenBank,登录号EU643833)。经BLAST分析,结果表明,该分离株的16 S rRNA基因核苷酸序列与GenBank上登录的奇异变形杆菌分离株(AY820623、EF091150)的同源性为99.7%,证实该分离菌株为狐狸奇异变形杆菌,并命名为HU/08。致病性试验证明,该分离菌株对小白鼠有高致病性;毒素测定试验证明,该分离菌培养液的无菌滤液对小白鼠无毒性作用。     

石胆酸诱发豚鼠胆囊炎动物模型的病理学研究

以酶病理组织化学方法结合胆汁生化分析，研究了石胆酸（ＬＣＡ）诱发豚鼠胆囊炎和胆结石的形成过程中，肝胆系统内源性β葡萄糖苷酸酶（βＧＣＤ）、酸性粘多糖及多种胆汁成分的变化。结果表明，ＬＣＡ能造成肝损伤，引起豚鼠增生性胆囊炎病变；肝和胆囊中内源性βＧＣＤ活性明显升高；胆汁βＧＣＤ含量显著升高，且与ＵＣＢ／ＴＢ比值显著正相关。     

东北亚地区科技合作的路径选择——以大连与日、韩、俄科技合作为研究视角

东北亚地区科技实力较强，区域内各国科技优势互补，各有所长，各有所需，各国政府都十分重视国际科技合作。近年来，为了提升科技产业国际化水平，大连不断加强与东北亚地区的科技合作。大连与东北亚地区的科技合作具有十分重要的战略地位。因此，应抓住机遇，大力推进大连与东北亚地区科技合作的创新升级。