نتایج جستجو برای: chelex 100

تعداد نتایج: 415337  

Journal: :iranian red crescent medical journal 0
mahsa tabibnejad department of immunology and microbiology, arak university of medical sciences, arak, ir iran mohammad yousef alikhani brucellosis research center, hamadan university of medical sciences, hamadan, ir iran; brucellosis research center, hamadan university of medical sciences, hamadan, ir iran. tel: +98-9125443147, fax: +98-8132533936, e-mail:; mohammad arjomandzadegan, tuberculosis and pediatric infectious research center and department of microbiology, arak university of medical sciences, arak, ir iran. tel: +98-9188602576, fax: +98-8634173518 mohammad arjomandzadegan tuberculosis and pediatric infectious research center and department of microbiology, arak university of medical sciences, arak, ir iran; brucellosis research center, hamadan university of medical sciences, hamadan, ir iran. tel: +98-9125443147, fax: +98-8132533936, e-mail:; mohammad arjomandzadegan, tuberculosis and pediatric infectious research center and department of microbiology, arak university of medical sciences, arak, ir iran. tel: +98-9188602576, fax: +98-8634173518 seyed hamid hashemi brucellosis research center, hamadan university of medical sciences, hamadan, ir iran zahra naseri blood transfusion research center, high institute for research and education in transfusion, hamadan, ir iran

conclusions the results prove that the presented double pcr method could be used to detect positive cases from culture-negative blood samples. the chelex 100 method is simpler and safer than the use of qiagen kit for dna extraction. materials and methods a total of 100 patients with suspected brucellosis were included in this experimental study and given positive serological tests. diagnosis wa...

Journal: :Nucleic acids research 1999
N J Coombs A C Gough J N Primrose

Archival, formalin-fixed, paraffin-embedded tissue is an invaluable resource for molecular genetic studies but the extraction of high quality nucleic acid may be problematic. We have optimised DNA extraction by comparing 10 protocols, including a commercially available kit and a novel method that utilises a thermal cycler. The thermal cycler and Chelex-100 extraction method yielded DNA capable ...

2013
R. Fromme G. Renger

The mechanism of atrazine binding and its modification by Chelex-100-induced Ca2+ deple­ tion and proteolytic degradation by trypsin, was analyzed in PS II membrane fragments from spinach. It was found: 1) Chelex-100 treatment leads in a comparatively slow process (/, 2 = 5 — 10 min) to Ca2+ re­ moval from a site that is characterized by a high affinity as reflected by Ku values of the order of...

2017
Huda H. Al-Griw Zena A. Zraba Salsabiel K. Al-Muntaser Marwan M. Draid Aisha M. Zaidi Refaat M. Tabagh Mohamed A. Al-Griw

Efficient extraction of genomic DNA (gDNA) from biological materials found in harsh environments is the first step for successful forensic DNA profiling. This study aimed to evaluate two methods for DNA recovery from animal tissues (livers, muscles), focusing on the best storage temperature for DNA yield in term of quality, quantity, and integrity for use in several downstream molecular techniq...

Journal: :The Medical journal of Malaysia 2010
C S Edwin Shiaw M S Shiran Y K Cheah G C Tan A R Sabariah

This study was done to evaluate various DNA and RNA extractions from archival FFPE tissues. A total of 30 FFPE blocks from the years of 2004 to 2006 were assessed with each modified and adapted method. Extraction protocols evaluated include the modified enzymatic extraction method (Method A), Chelex-100 extraction method (Method B), heat-induced retrieval in alkaline solution extraction method ...

Journal: :Genetics and molecular research : GMR 2014
E C B Silva M A Pelinca A C Acosta D M F Silva M A Gomes Filho M M P Guerra

Successful DNA extraction is indispensable for molecular methods based on polymerase chain reaction (PCR); however, goat sperm DNA extraction is limited. Thus, the aim of this study was to evaluate three methods to extract DNA from goat sperm for use in PCR. Eight goat semen pools were used for DNA extraction by using the DNeasy Blood & Tissue Kit, phenol-chloroform, and Chelex-100 methods. DNA...

Journal: :Journal of clinical pathology 1994
X de Lamballerie F Chapel C Vignoli C Zandotti

With both a classic DNA preparation protocol (including removal of paraffin wax and protein digestion) and a DNA extraction protocol with Chelex 100, the hepatitis B virus genome was searched for using the polymerase chain reaction (PCR) in 30 samples of paraffin wax embedded liver tissue from patients with chronic hepatitis. The classic protocol was more sensitive than the rapid Chelex 100 pro...

Journal: :Forensic science international 1996
D Sweet M Lorente A Valenzuela J A Lorente J C Alvarez

Recovery, preservation and analysis of body fluid stains is an important aspect of forensic science. PCR-based typing of DNA extracted from recovered stains is often a crucial method to identify a perpetrator or exclude an innocent suspect. This paper reports an improved method of extracting genomic DNA from saliva stains deposited on human skin in simulated bite mark situations. Results of org...

2009
Mônica Wallner-Kersanach Carlos Francisco F. de Andrade Hao Zhang Márcio R. Milani Luis Felipe H. Niencheski

A técnica de gradiente difusivo de membrana (DGT) foi utilizada para determinar metais lábeis in situ durante diferentes condições hidrológicas no estuário da Lagoa dos Patos. As amostras de água foram também analisadas para a fração lábil-Chelex para Cd, Co, Cu, Mn, Ni e Zn usando resina Chelex-100. As concentrações lábeis-DGT de Cd, Cu, Ni e Zn foram mais baixas que a lábil-Chelex, possivelme...

Journal: :Applied and environmental microbiology 1993
M Abbaszadegan M S Huber C P Gerba I L Pepper

Standard methods for the detection of enteroviruses in environmental samples involve the use of cell culture, which is expensive and time-consuming. The polymerase chain reaction (PCR) is an attractive method for the detection of enteroviruses in water because primary cell culture is not needed and the increased sensitivity of PCR allows detection of the low numbers of target DNAs and RNAs usua...

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