1.Probe technology and application of fluorescence molecular imaging
Huangsheng PU ; Bin ZHANG ; Fei LIU ; Xin LIU ; Jing BAI
International Journal of Biomedical Engineering 2012;35(4):220-223
In recent years,fluorescent probes become more available for the progress of biology and gene technology,which has accelerated the development of fluorescence molecular imaging.With these fluorescent probes,target molecular,protein and gene can be specifically located and analyzed,which make possible the early detection and treatment of disease.This paper gives an introduction of the fluorescent probe technology and its application in the fields of biology and medicine.
2.Specific PCR Identification of Hibisci Cortex and Its Adulterants Based on DNA Signature Sequence Tags
Yanan LIU ; Zhongyi HUA ; Yuyang ZHAO ; Yan JIN ; Huangsheng PENG ; Chao JIANG ; Jingzhe PU ; Yuan YUAN
Chinese Journal of Experimental Traditional Medical Formulae 2022;28(17):133-139
ObjectiveUncommon medicinal herbs are valuable medicinal resources, but their identification is a difficult problem in Chinese medicine due to their particularity and complexity. It is, therefore, urgent to establish a method for the identification of uncommon medicinal herbs. In this study, DNA signature sequence (DSS) tags were used to establish a specific polymerase chain reaction (PCR) identification method for Hibisci Cortex, the origin plant of Hibisci Cortex, and its adulterants. MethodThe candidate DSS tags were obtained from the chloroplast genome sequence analysis, and the DSS tags were verified by DNA sequencing. The specific identification primers for H. syriacus were designed based on the obtained reliable DSS tags. The PCR reaction conditions were optimized, and the tolerance and feasibility were investigated. ResultA DSS tag for identification of H. syriacus was obtained from the comparison of sequencing results of the amplified products with DSS, which revealed the distinguishing characteristics of Hibisci Cortex and its adulterants. A pair of specific primers for H. syriacus was designed according to the DSS tag. After PCR amplification and gel electrophoresis with the primers, a single bright band of about 270 bp was observed from H. syriacus, which did not appear in the four adulterants. ConclusionA DSS tag obtained in this study can be used to identify H. syriacus. The specific primers designed based on this DSS tag can accurately and simply identify the original plant of Hibisci Cortex and its adulterants, which provides a new method and idea for the molecular identification of genuine and counterfeit products of Hibisci Cortex.