نتایج جستجو برای: تکنیکhigh resolution melting

تعداد نتایج: 308182  

Journal: :Clinical chemistry 2003
Cameron N Gundry Joshua G Vandersteen Gudrun H Reed Robert J Pryor Jian Chen Carl T Wittwer

BACKGROUND Common methods for identification of DNA sequence variants use gel electrophoresis or column separation after PCR. METHODS We developed a method for sequence variant analysis requiring only PCR and amplicon melting analysis. One of the PCR primers was fluorescently labeled. After PCR, the melting transition of the amplicon was monitored by high-resolution melting analysis. Differen...

2014
Zahra Vali Abbasali Raz Hanieh Bokharaei Mohammad Nabavi Mohammad Hassan Bemanian Mina Sharifi Yazdi Navid Dinparast Djadid

BACKGROUND Asthma is caused by the combination of different factors. Current concepts of asthma pathogenesis emphasize on gene-environment interactions. Mega-genome scanning projects revealed that different Single Nucleotide Polymorphisms (SNPs) are related to asthma susceptibility. rs7216389-T is one of them that is related to childhood asthma and its effect on childhood asthma severity has be...

حسینی, سیدجمال, شریفی, شهرآشوب, میری نرگسی, میرساعد, ناظمی, علی, هاشمی, مهرداد,

سابقه و هدف: آنالیز HRM (High Resolution Melting) تکنیکی است که میزان کاهش فلورسنت را در طی فرایند شیب حرارتی ذوب DNA در اثر خروج رنگ اندازه‌گیری می‌نماید. ژن STK11 یکی از پروتئین‌های خانواده سرین- ترئونین کیناز سلولی را رمز می‌نماید که تنظیم کننده قطبیت سلولی بوده و هم‌چنین به عنوان پروتئین مهار کننده تومور عمل می‌نماید. موتاسیون‌های ژرم لاین در این ژن همراه با سندروم Peutz-Jeghers واستعدا...

2013
Yanfang Zhu Qitian Wang Jin Hu Liwei Zhu Jiancheng Wang Shuijin Zhu Yajing Guan

Rice (Oryza sativa L.) is one of the most important crops in the world. It is essential to develop an efficient method to build the fingerprinting database of commercial hybrid rice cultivars and their parental lines in seed market for rapid and unambiguous cultivar identification and seed purity analysis as new similar cultivars increasing yearly. The objective of this investigation were to fi...

Journal: :Clinical chemistry 2004
Luming Zhou Alexander N Myers Joshua G Vandersteen Lesi Wang Carl T Wittwer

BACKGROUND Homogeneous PCR methods for genotyping usually require fluorescently labeled oligonucleotide probes. Amplicon melting with the DNA dye LCGreen I was recently introduced as a closed-tube method of genotyping that does not require probes or real-time PCR. However, some single-nucleotide polymorphisms (SNPs) could not be completely genotyped without addition of a known genotype, and hig...

Journal: :Clinical chemistry 2004
Michael Liew Robert Pryor Robert Palais Cindy Meadows Maria Erali Elaine Lyon Carl Wittwer

BACKGROUND High-resolution melting of PCR amplicons with the DNA dye LCGreen I was recently introduced as a homogeneous, closed-tube method of genotyping that does not require probes or real-time PCR. We adapted this system to genotype single-nucleotide polymorphisms (SNPs) after rapid-cycle PCR (12 min) of small amplicons (</=50 bp). METHODS Engineered plasmids were used to study all possibl...

Journal: :Clinical chemistry 2003
Carl T Wittwer Gudrun H Reed Cameron N Gundry Joshua G Vandersteen Robert J Pryor

BACKGROUND High-resolution amplicon melting analysis was recently introduced as a closed-tube method for genotyping and mutation scanning (Gundry et al. Clin Chem 2003;49:396-406). The technique required a fluorescently labeled primer and was limited to the detection of mutations residing in the melting domain of the labeled primer. Our aim was to develop a closed-tube system for genotyping and...

Background: Colorectal cancer (CRC) is the third most common cancer worldwide. microsatellite instability (MSI) is a molecular marker of a deficient mismatch repair system and happens in almost 15% of CRCs. Because of a wide frequency of MSI+ CRC in Iran compared to other parts of the world, the importance of screening for this type of cancer is highlighted. Methods: The most common MSI detecti...

Beta-thalassemia is one of the most common autosomal recessive disorders in the world population resulting from over 200 different mutations of HBB gene. Beta-thalassemias are caused by point mutations or, more rarely, deletions in the HBB gene leading to reduced (beta+) or absent (beta0) synthesis of the beta chains of hemoglobin (Hb). High-resolution melting of polymerase chain reaction (PCR)...

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