Hermetia illucens in diets for zebrafish (Danio rerio): A study of bacterial diversity by using PCR-DGGE and metagenomic sequencing. [PDF]
Osimani A +14 more
europepmc +1 more source
PCR-DGGE applied to microbial ecology that influence the production of OTA [PDF]
In tropical zones, OTA is mainly produced in coffee beans by three Aspergillus species: A. carbonarius, A. niger section Nigri and A. ochraceus section Circumdati. Among them, the most important OTA producer and the most frequently isolated is A. carbonarius. In temperate zones Penicillium verrucosum and P.
Durand, Noël +3 more
openaire
The correlation of crystalline and elemental composition of urinary stones with a history of bacterial infections: TXRF, XRPD and PCR-DGGE studies. [PDF]
Arabski M +9 more
europepmc +1 more source
Hidden mycota of pine needles: Molecular signatures from PCR-DGGE and Ribosomal DNA phylogenetic characterization of novel phylotypes. [PDF]
Jeewon R +6 more
europepmc +1 more source
PCR-DGGE Analysis: Unravelling Complex Mixtures of Badnavirus Sequences Present in Yam Germplasm. [PDF]
Turaki AA +4 more
europepmc +1 more source
Cider Apple Native Microbiota Characterization by PCR-DGGE [PDF]
Sergio Alonso +4 more
openaire +1 more source
變性梯度膠體電泳分析( DGGE; Denaturing Gradient Gel Electrophoresis )在遺傳上的應用
變性梯度膠體電詠分析(DGGE;Denaturing Gradient Gel Electrophoresis),是以DNA的變性原理為基礎而偵測DNA變異的一種生物技術。DGGE偵測DNA的變異有高度靈敏及精確性,因此在人類遺傳疾病的偵測上效果優越,所以目前為止以動物及醫學研究應用DGGE技術較多,植物方面僅有小麥及玉米有這方面的報導。在作物的育種工作中常因DNA標誌多型性不易取得,而使育種工作不易進行。RFLP及RAPD雖然已大量的應用於作物的育種工作中 ...
Woo-Nang Chang +5 more
core
PCR-DGGE analysis of population dynamics of lactic acid bacteria in kimchi by addition of bacteriocins. [PDF]
Jeong M, Kim J, Choi E, Kim JS, Kim WJ.
europepmc +1 more source
Use of the PCR-DGGE Method for the Analysis of the Bacterial Community Structure in Soil Treated With the Cephalosporin Antibiotic Cefuroxime and/or Inoculated With a Multidrug-Resistant Pseudomonas putida Strain MC1. [PDF]
Orlewska K +2 more
europepmc +1 more source
建立了通过PCR-DGGE研究钉螺体内细菌群落结构的方法,并采用此技术分析了钉螺体内细菌群落结构。钉螺样本采自湖北省荆州市,样本带回实验室经破壳解剖后取清洗的钉螺内脏放入无菌离心管后经酚-氯仿法抽提微生物DNA。使用获得的微生物DNA为模板,选择细菌原核通用引物F357-GC和R518进行PCR扩增得到大约250bp的目的片段,然后采用变性梯度凝胶电泳结合DNA测序技术对获得的目的片段进行分析。结果显示此技术能够区分幼螺和成螺体内细菌群落结构差异 ...
胡合华, 余育和, 倪加加
core

