نتایج جستجو برای: pet22b expression vector

تعداد نتایج: 1048484  

aboarhman emamzadeh, mojtaba mortazavi, Saman Hosseinkhani,

Introduction: Gene expression and purification of luciferases from the firefly, Lampyris turkestanicus, and optimization of cellular ATP measurements were performed. Methods: cDNA encoding luciferases from Lampyris turkestanicus was transferred from pQE30 vector into pET28a expression vector and pLtu28 was built. Newly constructed vector was expressed in E. coli XL1 Blue and the recombinant l...

Journal: :jundishapur journal of microbiology 0
mojtaba fattahi abdizadeh infectious and tropical diseases research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; department of virology, institute pasteur of iran, tehran, ir iran manoochehr makvandi infectious and tropical diseases research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; department of virology, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; infectious and tropical diseases research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran. tel: +98-6113738313, fax: +98-6113738313 alireza samarbafzadeh department of virology, ahvaz jundishapur university of medical sciences, ahvaz, ir iran kayhan azadmanesh department of virology, institute pasteur of iran, tehran, ir iran

conclusions according to the high functionality of the produced recombinant vector, it seems a good applicable tool for making an indicator cell line in subsequent basic and drug studies. results recombinant vector, pgl4ltr-luc, has expression levels of more than 50 folds compared to the control when co-transfected with the tax expressing vector into hek 293t cells. moreover, cells display more...

Journal: :physiology and pharmacology 0
saman hosseinkhani biochemistry department, faculty of basic sciences, tarbiat modares university, tehran, iran mojtaba mortazavi biochemistry department, faculty of basic sciences, tarbiat modares university, tehran, iran aboarhman emamzadeh biochemistry department, faculty of basic sciences, tarbiat modares university, tehran, iran

introduction: gene expression and purification of luciferases from the firefly, lampyris turkestanicus, and optimization of cellular atp measurements were performed. methods: cdna encoding luciferases from lampyris turkestanicus was transferred from pqe30 vector into pet28a expression vector and pltu28 was built. newly constructed vector was expressed in e. coli xl1 blue and the recombinant luc...

Creatinine amidohydrolase(EC 3.5.2.10) catalyzes the reversible conversion of creatinine to creatine. Creatininase in combination with other enzymes is used for detection of creatinine in serum and urine which is of significant value for detection of renal, muscular and thyroid functions. The aim of this study was to produce recombinant creatininase enzyme in E.coli expression system to use it ...

Ahanjan M Amiri Yekta A Azizzadeh Pormehr L Bahraminejad E Ebrahimi S Eskandari Nasab MP Fatemi N Gourabi H Sanati MH

Background: Follicle stimulating hormone is a heterodimeric protein composed of two subunits, α and ß, which are linked noncovalently. The hypophysial gonadotropin FSH plays an important role in the regulation of oocyte maturation, and a key component for growth of ovulator follicles in ewes. Materials and Methods: This study seeks to clone and express the ovine follicle stimulating hormone sub...

آزادی, یعقوب, احمدپور, احسان, اسپوتین, عادل, دریانی, احمد, رجبی, صبا, شانه بندی, داریوش, علیزاده, پریا, محامی اسکویی, محمود, کاظمی, توحید,

Background and purpose: Toxoplasma gondii (T. gondii) is an obligatory intracellular protozoan parasite. Toxoplasmosis is highly prevalent and has a great effect on public health, therefor, there is a need for vaccine and sensitive diagnostic procedures. This study aimed at cloning and investigating the expression of ROP13 gene of T. gondii. Materials and methods: In this study, the gene was c...

Ali Bahrami Ali Reza Saeedinia Ebrahim Vasheghani Farahani, Jafar Mohammadian-Mosaabadi Rasoul Khalilzadeh Seyed Abbas Shojaosadati,

Human granulocyte-colony stimulating factor (hG-CSF) cDNA was expressed in the methylotrophic yeast Pichia pastoris under the control of the alcohol oxidase (AOX1) promoter. An expression vector for hG-CSF secretion was constructed using vector pPIC9. Higher levels of hG-CSF was obtained using a P. pastoris Mut+ (methanol utilization fast) phenotype. The effects of environmental factors such as...

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...

Many researchers adopt Local Binary Pattern for pattern analysis. However, the long histogram created by Local Binary Pattern is not suitable for large-scale facial database. This paper presents a simple facial pattern descriptor for facial expression recognition. Local pattern is computed based on local gradient flow from one side to another side through the center pixel in a 3x3 pixels region...

Journal: Vaccine Research 2015
A Ataei- Pirkooh , F Goudarzifar , H Keyvani , M Eslami, MR Aghasadeghi , R Vahabpour , SH Monavari ,

Introduction: Glycoprotein B (gB) is the major antigen for induction of humoral responses against human cytomegalovirus (HCMV) making it an attractive candidate for immune prophylaxis. In the present study, the humoral immune response of BALB/c mice to a truncated HCMV gB protein fused with GFP was evaluated. Methods: The truncated gB coding sequence was synthesized and cloned in pEGFPN1 eukary...

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