محمد هادی سخاوتی

استادیار، گروه علوم دامی، دانشکده کشاورزی، دانشگاه فردوسی مشهد.

[ 1 ] - بررسی ساختار ژنتیکی بخشی از ناحیه پروموتر در ژن لاکتوفورین درشترهای تک کوهانه و دو کوهانه ایران

شیر شتر یکی از منابع پروتئینی غنی به شمار می آید. لاکتوفورین یکی از پروتئین های مهم آب پنیر شیر شتر می باشد. نواحی پروموتری، نواحی هستندکه در بیان ژن اهمیت ویژه ای دارند. هدف از این تحقیق بررسی ساختار ژنتیکی بخشی از ناحیه پروموتر ژن لاکتوفورین به طول 790 نوکلئوتید، بین دو گونه شتر تک کوهانه و دو کوهانه ایران بود.10 نمونه خون از شتر تک کوهانه و 5 نمونه خون از شتر دو کوهانه جمع آوری شد. ناحیه مور...

[ 2 ] - Cloning and molecular characterization of Omp31 gene from Brucella melitensis Rev 1 strain

Brucellosis, caused by the genus Brucella bacterium, is a well-known infection among domestic animals. Considering the serious economic and medical consequences of this infection, various preventive efforts have been made through using recombinant vaccines, based on outer membrane protein (OMP) antigens of Brucella species. The objective of the present study was to clone, analyze the sequence, ...

[ 3 ] - An optimized affordable DNA-extraction method from Salmonella enterica Enteritidis for PCR experiments

In diagnostic and research bacteriology settings with budget and staff restrictions, fast and cost-effective genome extraction methods are desirable. If not inactivated properly, cellular and/or environmental DNA nucleases will degrade genomic material during the extraction stage, and therefore might give rise to incorrect results in PCR experiments. When crude cell extracts, proteinase K–treat...

[ 4 ] - Cloning, molecular analysis and epitopics prediction of a new chaperone GroEL Brucella melitensis antigen

Objective(s):Brucellosis is a well-known domestic animal infectious disease, which is caused by Brucella bacterium. GroEL antigen increases Brucella survival and is one of the major antigens that stimulates the immune system. Hence, the objective of the present study was cloning and bioinformatics analysis of GroEL gene. Materials and Methods: The full-length open reading frame of this gene was...

[ 5 ] - Polymorphism of the SCNN1g Gene and its Association with Eggshell Quality

Eggshell quality is the main trait to assess egg quality. Marker assisted selection can be used to improve this trait. During eggshell formation, a mass of inorganic minerals is deposited. The Sodium Channel (SCNN1) gene family plays an essential role in cation transportation and SCNN1g is a member of this gene family. The objective of this study was to estimate the frequency of SCNN1g gene var...

[ 6 ] - Identification of a Specific Pseudo attP Site for Phage PhiC31 Integrase in Bovine Genome

Background: PhiC31 integrase system provides a new platform in various felid of research, mainly in gene therapy and creation of transgenic animals. This system enables integration of exogenous DNA into preferred locations in mammalian genomes, which results in robust, long-term expression of the integrated transgene. Objectives: Identification of a novel pseudo attP site. Materials and Methods...

[ 7 ] - Design and Production of a Novel Recombinant Chimeric IL2-Omp31 Antigen against Brucella Infection

Brucellosis is a zoonotic disease in human and animals. Brucella melitensis is one of the most pathogenic species of Brucella in goat and sheep. Omp31 is an outer membrane protein of Brucella that acts as an immunogenic protein. Cytokines are glycoproteins with low molecular weight that play the role of an immune adjuvant and regulate immune responses. Interleukin-2 is one of the most important...

[ 8 ] - Production of Brucella lumazine Synthase Recombinant Protein to Design a Subunit Vaccine against Undulant Fever

Brucella bacterium causes Brucellosis, an infectious disease spreading from animals to human. Brucella lumazine synthase (BLS) is a highly immunogenic protein with adjuvant properties, which has been introduced as an effective protein carrier for vaccine development. This protein also plays a significant role in inducing immune system. This study aimed to clone, express, and purify the BLS gene...