نتایج جستجو برای: nested quantitative pcr

تعداد نتایج: 483813  

A. Ahoonmanesh M. Bahar M. Sharbatkhari,

Pear decline is a very important phytoplasma disease that causes considerable quantitative and qualitative losses to this fruit crop. Due to economical importance of pear in Isfahan province, Iran, and the difficulty to determine the occurrence of the disease simply based on symptoms in orchards, a detection method for the phytoplasma causing disease in pears in the region was developed. Since ...

Journal: :modares journal of medical sciences: pathobiology 2007
kiana shahzamani farzaneh sabahi shahin merat houri rezvan siamak mirab samiee

objective: hepatitis c virus is the major cause of viral hepatitis and its diagnosis in suspected specimens is of great importance. the risk of transfusion- transmitted virus infection is primarily the result of failure in serological screening tests to detect recently infected donors in the pre-seroconversion window period of infection. therefore, sensitive and accurate diagnosis of hcv prior ...

Journal: :American journal of clinical pathology 2002
Ralf Bialek Friederike Ernst Klaus Dietz Laura K Najvar Jürgen Knobloch John R Graybill Gundula Schaumburg-Lever

To optimize diagnosis of histoplasmosis in tissue sections, 30 spleen specimens from mice, experimentally infected with Histoplasma capsulatum, were examined by H&E, Grocott stain, anti-bacille Calmette-Guerin antibody immunostain, Fungiqual A fluorochrome stain (Drs Reinehr and Rembold, Kandern, Germany), and a nested polymerase chain reaction (PCR) assay. Results were compared with the tissue...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شهید باهنر کرمان - دانشکده دامپزشکی 1391

توکسوپلاسما گوندئی تک یاخته ای داخل سلولی و رایج ترین انگل مشترک بین انسان و دام است. مصرف اوسیست های محیطی (مثل خوردن آب و سبزی آلوده) و همچنین خوردن گوشت خام (که کیست انگل در نسوج آن وجود دارد) راه اصلی انتقال انگل به انسان و احشام می باشد. تاکنون روشهای مختلفی مانند سابین فلدمن، nested pcr، real time pcr و pcr- rflpبرای شناسایی این انگل در گوشت های آلوده بکار رفته است. هدف اصلی این مطالعه ب...

Background and Aim:  PCR has high sensitivity and specificity for the determination offungal DNA. It is also useful for rapid identification of the most common species of Aspergillus. The purpose of this study was to compare culture method with nested PCR method to determine Aspergillesion in diabetic foot patient in Imam Khomeini Hospital, Tehran. Material and Methods: Sixty-five case...

2015

Check out our Selection Guide! PCR RNA DNA LAMP KitsOne Tube For Superior Reproducibility. From fish tissues or fluids using a nested PCR primer set. The use of trade, firm, or corporation names in this protocol is for the information and.jor consideration in designing a nested PCR protocol compatible with quantitation is to assure that the maximum concentration of PCR products produced by the....

Journal: :International Journal of Infectious Diseases 2021

ObjectivesOne of the problems encountered in malaria control and elimination is inaccurate diagnosis, resulting from degree sensitivity different diagnostic tools. Even though microscopy remains gold standard for more sensitive robust tools such as polymerase chain reactions (PCR) are used research settings to monitor interventions track sub-microscopic infections due some drawbacks microscopy....

Journal: :The American journal of tropical medicine and hygiene 2007
Chulmin Kim Hiroshi Iseki Maria Shirley Herbas Naoaki Yokoyama Hiroshi Suzuki Xuenan Xuan Kozo Fujisaki Ikuo Igarashi

Two TaqMan-based real-time polymerase chain reaction (PCR) assays devised for the detection of two bovine Babesia parasites, Babesia bovis and B. bigemina, were evaluated for their diagnostic utility using cultured parasites and 92 field bovine blood samples collected from cattle living in Brazil. The real-time PCR assays were compared with previously established nested-PCR assays. The detectio...

ژورنال: تحقیقات دامپزشکی 2008
ترانه حاجیان دینا مرشدی سید علی قرشی, محسن لطفی, مرتضی دلیری جوپاری‌

در این مطالعه یک روش Nested-PCR ‌برای تشخیص دو ویروس BVDV ‌از سویه NADL ‌بهینه سازی گردید. در آزمایش RT-PCR، قسمتی از منطقه غیر قابل ترجمه ناحیه ‌‌'5 ‌ویروس به طول 249 جفت باز تکثیر شد. محصول PCR در وکتور R/T57pTZ کلون گردید و نتیجه تعیین ردیف اسیدهای نوکلوتیدی آن اختصاصی بودن آزمایش را تایید نمود. سپس پرایمرهای داخلی انتخاب و آزمایش Nested-PCR ‌انجام گردید و یک قطعه DNA ‌به طول 155 جفت باز تکث...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید