TD-RAPD技术用于罂粟品种鉴定初探

目的探索TD-RAPD技术用于罂粟品种鉴定的可行性。方法采用改良CTAB法从罂粟叶片中提取DNA;TD-RAPD技术对种植于云南西双版纳地区的1个罂粟样品进行扩增分析。结果建立了罂粟DNA提取方法,从10个随机引物中筛选出6个引物用于罂粟TD-RAPD分析。结论TD-RAPD技术可用于罂粟DNA的分子标记,为罂粟DNA数据库建立提供技术方法,最终从DNA分子水平上追溯罂粟植物毒源。     

半导体纳米材料显现潜在手印技术的研究新进展

自纳米技术引入到法庭科学领域以来,因其独特的优势,拓宽了手印技术工作人员的思路,受到了国内外法庭科学家的青睐,成为当前国内外手印学科学家研究的热点。本文主要介绍了半导体纳米材料显现手印的概念特点,并就半导体纳米材料显现手印技术的发展历程和最新进展作了较为详细的归纳和总结。     

Validation studies of the ParaDNA® Intelligence System with artificial evidence items

Short tandem repeat (STR) profiling is one of the mostly used systems for forensic applications. In certain circumstances, STR profiling is time-consuming and costly, which potentially leads to delays in criminal investigations. LGC (Laboratory of the Government Chemist, UK) Forensics has developed a robust STR profiling platform called the ParaDNA^® Intelligence Test System which can provide early tactical intelligence and aid investigators in making informed decisions on sample prioritization for detection. Here, we validated the ParaDNA intelligence test for its application in forensic cases using a range of mock evidence items following guidelines set by the Scientific Working Group on DNA Analysis Methods (SWGDAM). Specifically, we tested the sensitivity and accuracy of the ParaDNA intelligence test, as well as the success rates for detecting mock samples and for use in case scenarios. Our findings demonstrate that the ParaDNA intelligence test generates useful DNA profiles, especially for samples such as blood, saliva, and semen that contain ample DNA, indicating the benefits of including ParaDNA as a prior step in forensic STR profiling pipelines.     

不同手法推拿天河水穴对外感患儿的即时退热效果比较

目的 观察天河水穴在不同操作手法下的即时退热效果。方法 将94例患儿按年龄分为清天河水组、取天河水组及打马过天河组,通过测定患儿腋下体温、症状总积分和不良事件积分,评价3组临床疗效和不良反应。结果 治疗后3 h,打马过天河组患儿腋下体温及症状总积分明显低于其他两组（P<0.05）,清天河水组、取天河水组患儿腋下体温及症状总积分的差异均无统计学意义（P>0.05）;清天河水组、取天河水组不良事件积分均显著低于打马过天河组（P<0.05）。结论 3种手法均有退热效果,但打马过天河手法的即时退热效果最佳,但易造成皮损,清天河水、取天河水手法安全可靠,退热效果无差异。     

Touch DNA collection from improvised explosive devices: A comprehensive study of swabs and moistening agents

Improvised explosive devices (IEDs) are used in devastating terrorist attacks worldwide and daily in Thailand. Touch DNA deposited during IED assembly are subjected to intense heat and pressure, resulting in rare events of usable DNA profiles obtained from real casework. No study has simultaneously evaluated both swab brands and moistening agents for touch DNA collection from substrates encountered in IED evidence. In this study, we investigated the effects of swab brands and moistening agents on DNA collection from adhesive tape, a common IED substrate. A full factorial design using four cotton swab brands (two forensic and two medical cotton swabs) and six moistening agents (DNA-free water, phosphate-buffered saline, ethanol, sodium dodecyl sulfate, isopropanol, and lysis buffer) was employed (24 total combinations). Using buffy coats, we found that DNA recovery depended on both swab brands and moistening agents (p < 0.05). The optimal method recovered significantly higher DNA amount from real IED cases compared to the standard Royal Thai Police method. Percentages of high partial profiles also increased. Our results changed the standard operating protocol of the Thai police. Other commonly found substrates from IED cases are being investigated to maximize the evidential value obtained from touch DNA.     

Estimating Individual Contributions to Complex DNA SNP Mixtures.,

High‐throughput sequencing (HTS) of large panels of single nucleotide polymorphisms (SNPs) provides an alternative or complimentary approach to short tandem repeats (STRs) panels for the analysis of complex DNA mixture forensic samples. For STRs, methods to estimate individual contribution concentrations compare capillary electrophoresis peak heights, peak areas, or HTS allele read counts within a mixture. This article introduces three approaches (mean, median, and slope methods) for estimating individual DNA contributions to forensic mixtures for HTS/massively parallel sequencing (MPS) SNP panels. For SNPs, the major:minor allele ratios or counts, unique to each contributor, were compared to estimate contributor proportion within the mixture using the mean, median, and slope intercept for these alleles. The estimates for these three methods were typically within 5% of planned experimental contributions for defined mixtures.     

口蹄疫病毒O型和A型交互反应性单克隆抗体的筛选与鉴定

不同血清型口蹄疫病毒(FMDV)之间不能产生交叉免疫保护,但是血清学的交叉反应确实存在。本研究旨在建立一种筛选型间交互反应性抗体的方法,以期为解析FMDV血清型间保守的抗原结构奠定基础。本方法主要依据单个B细胞抗体技术,首先采用两种不同的荧光染料FluoProbes 647H和Pacific Blue分别标记O型与A型FMDV 146S灭活抗原,然后利用流式细胞分选技术,从免疫牛外周血单个核细胞(PBMCs)中分选出结合两种抗原的特异性B细胞,通过单个B细胞抗体基因测定,获得Ig G抗体重链与轻链可变区编码序列,并将可变区基因插入含有牛IgG抗体恒定区的pcDNA3.4载体中,构建IgG抗体的重链与轻链表达质粒。将重链与轻链表达质粒共转染中国仓鼠卵巢悬浮细胞(CHO-S)进行完整抗体表达。结果显示,通过该方法获得了5株FMDV特异性单克隆抗体,其中4株(H64、R82、I16、R29)经间接免疫荧光(IFA)检测都可特异性识别O和A型FMDV;ELISA结果显示,H64、R82、I16与O、A型抗原均具有较好的亲合力;Western-blot结果显示,I16可特异性结合O、A型FMDV结构蛋白VP2中的线性表位,说明在衣壳蛋白VP2上存在血清型间保守的抗原表位,通过本研究进一步加深了对FMDV抗原结构的认识。     

高仿真制模伪造指印的识别研究

目的 探究高仿真制模伪造指印的识别方法.方法 选取多个印泥指印作为母版,分别采用曝光法制作指模,将母版指印与对应的伪造指印进行整体比较及显微比较.结果 伪造指印较母版指印尺寸存在差异、纹线略变粗、纹线间隔略变小、细节特征易黏连、细小痕迹及细微特征不反映或反映不全、单根纹线的墨迹分布平实且缺少细微漏白等.结论 识别伪造指...     

新型手印提取器的研究

现场勘查中,技术人员对用粉末刷显的手印、灰尘加层手印拍照提取后,再用新型手印提取器提取效果更好。手印提取器使胶带与客体接触面积变小、压力均匀,从而避免在提取过程中产生气泡;同时,胶带具有粘性的一面与另一胶带紧密相粘,通过转动,能制成透明的手印检材,可直接通过印相放大、复印,或通过反差较大的衬底做背景进行比对鉴定。实践证明,运用手印提取器提取的手印具有高质量、手印特征反映好、保存时间长,而且在使用中方便简捷,提取速度快等优点。