نتایج جستجو برای: a dna fragment of 499 bp

تعداد نتایج: 23324543  

2007
J. L. VANNESTE

Strains of Pseudomonas syringae able to grow on minimal medium containing 500 mg/litre of copper sulphate were selected from a collection of streptomycin-resistant strains isolated in New Zealand. From one of these copper-resistant strains a 1.3 kb fragment of DNA was isolated by PCR using primers designed on genes reported to be associated with copper resistance. Sequencing of this fragment re...

آبانگاه, اسحق, زندی, محمد, سنجابی, محمد رضا, هادی تواتری, محمد حسین,

Prolactin is secreted from the anterior pituitary gland and plays an important role in the mammary gland development, differentiation and lactation. The aim of current study was to evaluate prolactin receptor gene polymorphisms in the Shal breed and Shal×Romanov crossbreeds. For this purpose, after blood sampling of animals and extraction of DNA using phenol chloroform method, two fragments of ...

Journal: :Nucleic acids research 1985
Y Kuchino F Mori S Nishimura

A 5 kbp DNA fragment containing the tRNAPro1 gene from Escherichia coli was cloned into Charon 21A phage and sequenced by the M13 DNA sequencing technique. When the cloned DNA fragment was used as a template for in vitro transcription with E. coli RNA polymerase, a tRNAPro1 precursor of 120 nucleotide residues was obtained. The tRNAPro1 gene transcribed as a single transcription unit was follow...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تحصیلات تکمیلی علوم پایه زنجان - دانشکده شیمی 1391

in this thesis a calibration transfer method is used to achieve bilinearity for augmented first order kinetic data. first, the proposed method is investigated using simulated data and next the concept is applied to experimental data. the experimental data consists of spectroscopic monitoring of the first order degradation reaction of carbaryl. this component is used for control of pests in frui...

Journal: :The international journal of biochemistry & cell biology 2004
Jesús M Torres Esperanza Ortega

A novel, accurate, rapid and modestly labor-intensive method has been developed to quantitate specific mRNA species by reverse transcription-polymerase chain reaction (RT-PCR). This strategy combines the high degree of specificity of competitive PCR with the sensitivity of laser-induced fluorescence capillary electrophoresis (LIF-CE). The specific target mRNA and a mimic DNA fragment, used as a...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Hammou Oubrahim Jun Wang Earl R Stadtman P Boon Chock

The activation of caspase-12 is involved in endoplasmic reticulum-mediated apoptosis. To investigate how caspase-12 is transcriptionally and translationally regulated, we isolated and sequenced the 5'-flanking region of mouse caspase-12 gene by a PCR-mediated chromosome-walking technique, using mouse genomic DNA as a template. Two DNA fragments of 3,221 and 800 bp were isolated and cloned into ...

Journal: :The American journal of tropical medicine and hygiene 1998
O P Perera A F Cockburn S E Mitchell J Conn J A Seawright

A genomic DNA library of Anopheles aquasalis Curry was screened for clones that hybridized more intensely to DNA from A. aquasalis than to DNA from A. benarrochi Gabaldon, Cova Garcia, and Lopez, A. konderi Galvao and Damasceno, A. nuneztovari Gabaldon cytotypes A, B, and C, A. oswaldoi (Peryassu), A. rangeli Gabaldon, Cova Garcia, and Lopez, or A. trinkae Faran. Two specific clones (2.5 kiloba...

K. Aghaiypour, S. Safavieh

  Leptospirosis is an acute infectious, systemic and septisemic disease which had recent outbreaks in some parts of Iran especially in north provinces. Rapid detection is a critical step for treatment and control of this disease. In this research a PCR based method was evaluated for detection of Iranian local endemic serovars. All reported endemic serovars of Leptospira including Leptospira gri...

DNA size markers are widely used to estimate the size of DNA samples on agarose or polyacrylamide gelelectrophoresis (PAGE). DNA markers can be prepared by mixing PCR products with definite sizes.Alternatively, they are prepared by restriction enzyme digestion of the genomic DNA of bacteriophages ornatural and synthetic DNA plasmids. The present study describes engineering of ...

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...

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