首页> 外文期刊>Dynamic Chiropractic >Real time sequence characterized amplified region (RT-SCAR) marker: Development and its application for authentication and quantification of Catharanthus roseus L. Don.
【24h】

Real time sequence characterized amplified region (RT-SCAR) marker: Development and its application for authentication and quantification of Catharanthus roseus L. Don.

机译:实时序列特征扩增区(RT-SCAR)标记:Catharanthus roseus L. Don的开发及其在鉴定和定量中的应用。

获取原文
           

摘要

The objective of the present study was to develop a Real Time-Sequence Characterized Amplified Region (RT-SCAR) ofCatharanthus roseus,an effective molecular marker for authentication and quantification. Here, we made a comparative study of SCAR and RT-SCAR marker. These newer RT-SCAR methods are useful for the correct identification and quantification ofC. roseus. In particular, this technique is very attractive and can be used as a novel tool for quantification of C. roseus when the SCAR results cannot be quantified and the RAPD results are not consistent. RAPD analysis of collected samples from different geographical locations in India was carried out with 25 random primers. The RAPD polymorphic band was cloned, sequenced and from the sequence information, primers pair for SCAR was developed. The same primers was used for RT-SCAR marker by using SYBR green fluorescence-based detection in Real Time PCR. Utilizing this newly specific RT-SCAR marker, we detected the presence and quantity ofC. roseusin all the analyzed several samples, by aiding 10% its substitute and adulterants at time of DNA isolation. No difference was found in pure sample and 10% adulterant sample with the help of SCAR but in the case of RT-SCAR difference was found in the DNA sample. This analytical strategy could be used further for large scale quantification ofC. roseus’smarket samples.
机译:本研究的目的是开发Catharanthus roseus的实时序列特征扩增区域(RT-SCAR),这是一种用于鉴定和定量的有效分子标记。在这里,我们对SCAR和RT-SCAR标记进行了比较研究。这些更新的RT-SCAR方法可用于正确鉴定和定量C。玫瑰。特别地,当无法量化SCAR结果且RAPD结果不一致时,该技术非常吸引人,并且可以用作定量玫瑰色念珠菌的新型工具。用25种随机引物对印度不同地理位置的采集样品进行了RAPD分析。克隆,测序了RAPD多态性条带,并从序列信息中,开发了SCAR的引物对。通过实时PCR中基于SYBR绿色荧光的检测,将相同的引物用于RT-SCAR标记。利用这种新的特异性RT-SCAR标记,我们检测了C的存在和数量。在分析DNA时,通过辅助10%的替代品和掺假品,可将所有分析样品中的roseusin分离出来。借助SCAR,在纯样品和10%掺假样品中均未发现差异,但在RT-SCAR的情况下,在DNA样品中未发现差异。这种分析策略可进一步用于C的大规模定量分析。玫瑰花市场样本。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号