نتایج جستجو برای: Nested-Splicing by Overlap Extension PCR

تعداد نتایج: 7204809  

Journal: :iranian journal of biotechnology 2015
ali asghar karkhane bagher yakhchali ferdous rastgar jazii bijan bambai saeed aminzadeh

background: splicing by overlap extension (soe) pcr is used to create mutation in the coding sequence of an enzyme in order to study the role of specific residues in protein’s structure and function.objectives: we introduced a nested-soe-pcr (n –soe-pcr) in order to increase the specificity and generating mutations in a gene by soe-pcr.  materials and methods: genomic dna from bacillus thermoca...

Background: Splicing by overlap extension (SOE) PCR is used to create mutation in the coding sequence of an enzyme in order to study the role of specific residues in protein’s structure and function. Objectives: We introduced a nested-SOE-PCR (N –SOE-PCR) in order to increase the specificity and generating mutations in a gene by SOE-PCR.   Materials and Methods: Genomic DNA from Bacillus thermo...

Journal: :Iranian journal of biotechnology 2015
Ali Asghar Karkhane Bagher Yakhchali Ferdous Rastgar Jazii Bijan Bambai Saeed Aminzadeh Fatemeh Rahimi

BACKGROUND Splicing by overlap extension (SOE) PCR is used to create mutation in the coding sequence of an enzyme in order to study the role of specific residues in protein's structure and function. OBJECTIVES We introduced a nested-SOE-PCR (N -SOE-PCR) in order to increase the specificity and generating mutations in a gene by SOE-PCR. MATERIALS AND METHODS Genomic DNA from Bacillus thermoc...

Background: Rotavirus group A (RVA) is recognized as a major cause of severe gastroenteritis in children and new-born animals. Nonstructural protein 4 (NSP4) is responsible for the enterotoxic activity of these viruses in the villus epithelial cells. Amino acids 114-135 of NSP4 are known to form the diarrhea-inducing region of this viral enterotoxin. Therefore, developing an NSP4 lacking the en...

کی, مریم, حجتی, زهره , حیدری, مریم ,

Background: Interferon beta is one of the most important members of group I interferons and is the main drug for multiple sclerosis treatment. Interferon beta has short half life and this compels patients to make frequent use of medicine. According to its clinical usage there is broad effort to improve translation level and protein production. There are several important factors which effect pr...

ژورنال: :مجله تحقیقات دامپزشکی (journal of veterinary research) 2015
سولماز ناصرلی تقی زهرایی صالحی بهار نیری فسایی علیرضا سعیدی نیا ایرج اشرافی تمامی

زمینه مطالعه: ایجاد موتاسیون در جایگاه اختصاصی می تواند یکی از روش های کارآمد جهت بررسی ویژگی و خواص تنظیمی ژن های گوناگون باشد. ﺑﺮوﺳﻠﻮز از ﻣﻬﻢ ﺗﺮﯾﻦ ﺑﯿﻤﺎریهای ﻋﻔﻮﻧﯽ ﻣﺸﺘﺮک ﺑﯿﻦ اﻧﺴﺎن و دام اﺳﺖ ﻛﻪ ﻣﻨﺠﺮ ﺑﻪ بروز ﺿﺮرهای اﻗﺘﺼﺎدی ﻓﺮاواﻧﻰ ﻣﻰ ﺷﻮد. ﺑﻨﺎﺑﺮاﯾﻦ ﺷﻨﺎﺳﺎﯾﯽ ﻋﻮاﻣﻞ پاتوژن و اﯾﻤﻨﯽ زا در جنس ﺑﺮوﺳﻼ ﺑﻪ ﻋﻨﻮان راهگشای ﺟﻬﺖ ﮐﻨﺘﺮل اﯾﻦ ﻣﻌﻀﻞ ﺑﻬﺪاﺷﺘﯽ ﻣﻄﺮح ﻣﯽ ﺑﺎﺷﺪ. هدف: با توجه به اهمیت جهش هدفدار در شناسایی ساخ...

Farzaneh Rabiee Hossein Baharvand Kamran Ghaedi Khadijeh Karbalaei Malihe Nazari Jahantigh Maryam Ostad Sharif Marzieh Nematollahi Mehran Miroliaei Mohamad Hossein Nasr Isfahani Shahnaz Razavi Somayeh Tanhaei

Epitope tagging is a method of expressing proteins whereby an epitope for a specific monoclonal antibody is fused to a target protein using recombinant DNA techniques. The aim of this study was to sub-clone the peroxisomal protein (PEP) cDNA into a mammalian expression vector leading to the formation of a  chimeric PEP-cDNA containing the FLAG epitope. The FLAG-PEP recombinant cDNA was construc...

Journal: :Indian Journal of Animal Research 2023

Background: In reverse genetics studies, minigenomes of negative sense RNA viruses are used to model the process virus replication and evaluate rescue system in course construction recombinant virus. current study, a minigenome (MG) for lentogenic D58 vaccine strain Avian orthoavulavirus 1 (AOAV-1) (Newcastle disease virus) was developed establish genetic this strain. Methods: The constructed b...

Mana Oloomi, Saeid Bouzari, Veladimir O. Rechinsky,

Four exons of the human genomic GM-CSF gene were assembled together using gene splicing by overlap extension (SOE) method. The resulting nucleotide sequence was cloned in the pET23a(+) ex‌pression vector under the control of strong bacteriophage T7 transcription and translation signals. The construct obtained was Transferred into the E. coli strain, BL21(DE3) pLysS and IPTG was used for inducti...

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