نتایج جستجو برای: hinfi

تعداد نتایج: 295  

Journal: :Biological & pharmaceutical bulletin 2009
Jeong Hoon Lee Jei Wan Lee Jung Sook Sung Kyong Hwan Bang Sung Gi Moon

The present study describes the molecular authentication of 21 Korean Artemisia species using PCR-RFLP (polymerase chain reaction-restriction fragment length polymorphism) technique based on the trnL-F sequences in chloroplast DNA. Five different banding patterns were generated from 21 Artemisia species using HinfI restriction enzyme. A. apiacea, A. keiskeana and A. sieversiana have specific ba...

Journal: :The Journal of general virology 1995
F Davidson P Simmonds J C Ferguson L M Jarvis B C Dow E A Follett C R Seed T Krusius C Lin G A Medgyesi

A method is described for identifying different genotypes of hepatitis C virus (HCV) by restriction endonuclease cleavage of sequences amplified by PCR from the 5' non-coding region. Using the enzymes HaeIII-RsaI and HinfI-MvaI, followed by cleavage with BstU1 or ScrFI, it was possible to identify and distinguish HCV genotypes 1a, 1b, 2a, 2b, 3a, 3b, 4, 5 and 6. The method was used to investiga...

1998
Edson Luis Maistro Fausto Foresti Claudio Oliveira

The absence of longitudinal bands in fish chromosomes has been associated with technical problems in chromosome preparations or the absence of a structural compartmentalization in the fish genome. In the present study, a R-banding pattern was obtained using a replication banding technique by in vivo treatment with 5-bromodeoxyuridine (5-BrdU). G-banding patterns were obtained after trypsin trea...

Journal: :Hayati Journal of Biosciences 2023

Toxoplasma gondii pathogenicity depends on the type derived from a clonal population. A genetic analysis of locus has been carried out to determine different genotypes T. (strain types I, II, and III) that are associated with human toxoplasmosis. The several linked toxoplasmosis have identified through study locus. In this investigation, PCR-RFLP was found be useful, simple method genotypic cha...

Journal: :Journal of Health and Allied Sciences NU 2022

Abstract Background Emergence of fluoroquinolone resistance in gut pathogens is a cause concern. Resistant to quinolone mainly due the point mutations at quinolone-resistance determining regions (QRDR). The aim study was develop polymerase chain reaction-restriction fragment length polymorphism assay (PCR-RFLP) detect QRDR gyrA and gyrB enteric pathogens. Methodology PCR-RFLP done for 83 region...

Journal: :Australian Journal of Grape and Wine Research 2021

Background and Aims To achieve both the control of undesirable yeasts improvement characteristics Merlot ‘Pago’ wines, Saccharomyces cerevisiae yeast diversity was investigated in a spontaneous fermentation from Utiel-Requena region (Spain). Isolates S. were characterised by holistic procedure using same grape must which they isolated. Methods Results Yeasts identified internal transcribed spac...

Journal: :Epidemiology and infection 2000
R E Sacco K B Register G E Nordholm

Fifty-seven bacterial isolates previously identified as Bordetella avium or B. hinzii were characterized by restriction enzyme analysis (REA) and/or ribotyping. Twenty restriction endonucleases were evaluated for REA. Digestion of chromosomal DNA from the 42 B. avium and 15 B. hinzii isolates with HinfI produced 8 and 7 distinct fingerprint profiles, respectively. Digestion with DdeI further di...

Journal: :Genetics and molecular research : GMR 2013
C Jiang Y Yuan M Chen L Huang

Authenticating multi-species original raw materials in commercial formulations is difficult. Jin Yin Hua and Shan Yin Hua, both classified as raw honeysuckle materials in the Chinese Pharmacopoeia, are used in various medicines. Differentiating one variety from another is difficult based on chemical analysis. We developed molecular authentication of multi-species original honeysuckle in 3 brand...

Journal: :Applied and environmental microbiology 1997
D Redecker H Thierfelder C Walker D Werner

A technique combining PCR and restriction fragment length polymorphism analysis was used to generate specific DNA fragment patterns from spore extracts of arbuscular mycorrhizal fungi. With the universal primers ITS1 and ITS4, DNA fragments were amplified from species of Scutellospora and Gigaspora that were approximately 500 bp long. The apparent lengths of the corresponding fragments from Glo...

Journal: :Journal of clinical pathology 1986
C A Ison C M Bellinger J Walker

DNA probe hybridisation was used to examine the relation between the cryptic plasmid from Neisseria gonorrhoeae and plasmids carried by pharyngeal isolates of Neisseria meningitidis and Neisseria lactamica. The complete gonococcal cryptic plasmid and HinfI derived digestion fragments subcloned into Escherichia coli were used to probe Southern blots of plasmid extracts. Homology was found to a p...

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