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<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>5</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2018</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Repair of Spinal Cord Injury; Mesenchymal Stem Cells as an Alternative for Schwann Cells</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>42</FirstPage>
			<LastPage>47</LastPage>
			<ELocationID EIdType="pii">75557</ELocationID>
			
<ELocationID EIdType="doi">10.29252/jabr.05.02.01</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mehrdad</FirstName>
					<LastName>Moosazadeh Moghaddam</LastName>
<Affiliation>Stem Cell and Regenerative Medicine Group, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-4645-8661</Identifier>

</Author>
<Author>
					<FirstName>Shahin</FirstName>
					<LastName>Bonakdar</LastName>
<Affiliation>National Cell Bank, Pasteur Institute of Iran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad Ali</FirstName>
					<LastName>Shokrgozar</LastName>
<Affiliation>National Cell Bank, Pasteur Institute of Iran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Shahab</FirstName>
					<LastName>Faghihi</LastName>
<Affiliation>Stem Cell and Regenerative Medicine Group, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2018</Year>
					<Month>03</Month>
					<Day>02</Day>
				</PubDate>
			</History>
		<Abstract>Spinal cord injury (SCI) is one of the most severe types of disabilities that has a limited capacity to repair; therefore, medical interventions are essential to the treatment of injuries. Cell transplantation is one of the remarkable strategies for the treatment of spinal cord injury. Transplantation of Schwann cells (SCs) has shown a great promising result for SCI but harvesting SC is limited due to donor complications and limited cell collection capacity. However, the use of stem cells to differentiate into SCs can reduce the risks associated with the use of mature cells in the grafting process. Mesenchymal stem cells can differentiate to various type cells. They are as easily accessed source with high growth rate and low immunogenicity; therefore, these properties make them an interesting source for cell therapy. These cells can be transdifferentiated into SC-like cells in neuronal induction media. Accordingly, many studies demonstrated that mesenchymal cells are well suited for cell therapy of SCI. This article briefly discusses the treatment of SCI by cell transplantation and the benefits of using Mesenchymal stem cells as an alternative for SCs.</Abstract>
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			<Param Name="value">Spinal cord injury</Param>
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			<Object Type="keyword">
			<Param Name="value">Cell Transplantation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Mesenchymal stem cell</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Schwann Cell</Param>
			</Object>
		</ObjectList>
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<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>5</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2018</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>A Review of Dietary Probiotics in Poultry</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>48</FirstPage>
			<LastPage>54</LastPage>
			<ELocationID EIdType="pii">76659</ELocationID>
			
<ELocationID EIdType="doi">10.29252/jabr.05.02.02</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Seyed Mohammad Ali</FirstName>
					<LastName>Aziz Mousavi</LastName>
<Affiliation>Applied Microbiology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Hamideh</FirstName>
					<LastName>Mahmoodzadeh Hosseini</LastName>
<Affiliation>Applied Microbiology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-3987-0164</Identifier>

</Author>
<Author>
					<FirstName>Seyed Ali</FirstName>
					<LastName>Mirhosseini</LastName>
<Affiliation>Applied Microbiology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-4065-7213</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2018</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</History>
		<Abstract>The use of probiotics has rapidly grown in recent years, enhancing the performance of broilers and leading to the production of products free of any probiotic trace. Recent evidence suggests that the use of microbial probiotics can play a significant role in the future of the poultry industry. Although this method is not complete yet, it can be employed by human societies as a useful tool to maximize poultry products, enhance the health, and ensure the safety of food sources. Some reports show that the application of probiotics in the feed of broilers can lead to positive outcomes such as increased weight and improved feed conversion ratio (FCR).</Abstract>
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			<Object Type="keyword">
			<Param Name="value">Probiotic</Param>
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			<Object Type="keyword">
			<Param Name="value">broiler</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Hen</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Turkey</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">growth</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Health</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_76659_2958ef004a18f50b380a87d1cfe5366d.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>5</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2018</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Essential Oil Composition and Antioxidant Activity of Calamintha officinalis Moench</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>55</FirstPage>
			<LastPage>58</LastPage>
			<ELocationID EIdType="pii">75328</ELocationID>
			
<ELocationID EIdType="doi">10.29252/jabr.05.02.03</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Fatemeh</FirstName>
					<LastName>Shams Moattar</LastName>
<Affiliation>Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Reyhaneh</FirstName>
					<LastName>Sariri</LastName>
<Affiliation>Deparment of Biology, University of Guilan, Rasht, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Masoud</FirstName>
					<LastName>Giahi</LastName>
<Affiliation>Department of Biology, Islamic Azad University, Lahijan Branch, Lahijan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Prichehreh</FirstName>
					<LastName>Yaghmaee</LastName>
<Affiliation>Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2017</Year>
					<Month>09</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;Introduction&lt;/strong&gt;: &lt;em&gt;Calamintha officinalis &lt;/em&gt;Moench (COM) is an aromatic herb from Lamiaceae family with high similarities to the common mints not only in its appearance but also in terms of aroma. The aim of this research was to evaluate antioxidant activity of plant extract and to identify constituents of its essential oil.&lt;br /&gt; &lt;strong&gt;Material and Methods&lt;/strong&gt;: The plant samples were collected from North of Iran (Guilan, Lahijan) and its identity was certified by a systematic botanist in University of Guilan. The dried leaves of COM were subjected to hydro-distillation using a Clevenger-type apparatus and the composition of the essential oil was analyzed by gas chromatography–mass spectrometry (GC-MS).&lt;br /&gt; &lt;strong&gt;Results: &lt;/strong&gt;It was found that major constituents of oil were trans-caryophyllene (8.55%), isomenthol (2.98%), tetrahydrolinalyl acetate (2.96%), and pinene (2. 24%). In other part of the research, the biological activities of superoxide dismutase (SOD) and catalase (CAT) were assayed by in extracts of the leaves spectrophotometric method. It was found the extract contained a considerable superoxide anion radical scavenging power. On the other hand, the biological activity of CAT in extract of COM leaves showed gradual increase during time with a gentle slope indicating an increase in oxidative stress.&lt;br /&gt; &lt;strong&gt;Conclusions&lt;/strong&gt;: The result of our study on &lt;em&gt;Calamintha &lt;/em&gt;revealed the existence of a specific component of the essential oil (trans-caryophyllene) that has not been reported by other researchers. In addition to the antioxidant property that was confirmed in this study, the major component of its essential oil was found to be an antimicrobial agent.</Abstract>
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			<Object Type="keyword">
			<Param Name="value">Calamintha officinalis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Enzymatic Antioxidants</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Essential oil</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_75328_8cdfa310a4be9e093e59ae737d4172de.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>5</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2018</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Isolation and Characterization of GDP-L-Galactose Phosphorylase Gene of Vitamin C Biosynthesis Pathway from Kiwi</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>59</FirstPage>
			<LastPage>63</LastPage>
			<ELocationID EIdType="pii">74249</ELocationID>
			
<ELocationID EIdType="doi">10.29252/jabr.05.02.04</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Soraya</FirstName>
					<LastName>Shiri</LastName>
<Affiliation>Campus of Agriculture and Natural Resources, Razi University, Kermanshah, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Alireza</FirstName>
					<LastName>Zebarjadi</LastName>
<Affiliation>Campus of Agriculture and Natural Resources, Razi University, Kermanshah, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-7091-3847</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2018</Year>
					<Month>01</Month>
					<Day>25</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;Introduction&lt;/strong&gt;: Vitamin C is a major antioxidant in plants and plays an important role in reducing the activity of reactive oxygen species. In humans, the main role of this molecule is the elimination of activity of active oxygen species along with being cofactor for many enzymes. Human is one of the few mammalian species that can not synthesize this vitamin and needs to get it through food sources. The GDP-L-galactose phosphorylase (&lt;em&gt;GGP&lt;/em&gt;) gene is one of the most important genes in the biosynthetic pathway of vitamin C, which codes for the GDPL-galactose phosphorylase enzyme. Isolation of &lt;em&gt;GGP &lt;/em&gt;gene is an important step in transferring it to elevate vitamin C biosynthesis in plants.&lt;br /&gt; &lt;strong&gt;Materials and Methods&lt;/strong&gt;: In current study, the isolation of this gene from kiwi plant was carried out and then was cloned in the pTG19-T plasmid via T/A cloning and subsequently sequenced to confirm it.&lt;br /&gt; &lt;strong&gt;Results&lt;/strong&gt;: Sequencing analysis of the &lt;em&gt;GGP &lt;/em&gt;gene showed that this fragment contains 1383 bp and the start and stop codons were ATG and TGA, respectively. The bioinformatics analysis of this gene can provide important information on gene and protein structure. The alignment of cloned sequence was done with other &lt;em&gt;Actinidia &lt;/em&gt;DNA sequences. The results based on neighbor-joining alignment showed that some of the mutations in nucleotides were related to the third nucleotide in a specific codon. Also, the minimum distance of protein sequences was observed between isolated &lt;em&gt;GGP &lt;/em&gt;and &lt;em&gt;Actinidia chinensis&lt;/em&gt;.&lt;br /&gt; &lt;strong&gt;Conclusions&lt;/strong&gt;: Based on analyses, isolated gene (&lt;em&gt;GGP&lt;/em&gt;) can be used for increase vitamin C content in other plants such as cucumber and for resistance to environmental stresses in different plants.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Actinida deliciosa</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">GDP-L-galactose phosphorylase (GGP) gene</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Kiwi</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">T/A cloning</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Vitamin C</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_74249_7f9d5084b8246feed7719e125b3834f6.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>5</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2018</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Identification and Ranking the Critical Success Factors of Business Incubator of Science and Technology Parks – A Case Study: Business Incubator of Baqiyatallah University of Medical Sciences</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>64</FirstPage>
			<LastPage>69</LastPage>
			<ELocationID EIdType="pii">75558</ELocationID>
			
<ELocationID EIdType="doi">10.29252/jabr.05.02.05</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mohammad Javad</FirstName>
					<LastName>Alishiri</LastName>
<Affiliation>Faculty of Management and Accounting, Islamic Azad University, Karaj Branch, Karaj, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Payam</FirstName>
					<LastName>Makvandi</LastName>
<Affiliation>Faculty of Management and Accounting, Islamic Azad University, Karaj Branch, Karaj, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Abbas</FirstName>
					<LastName>Khamesh</LastName>
<Affiliation>Faculty of Management and Accounting, Islamic Azad University, Karaj Branch, Karaj, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2018</Year>
					<Month>01</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;Introduction&lt;/strong&gt;: As part of national program of innovation and a part of the science-oriented development plan, “science and technology” parks have an effective role in accelerating the process of turning ideas into real products and thus, the development of technology by providing necessary conditions for market-oriented research and merchandising the outcome of research. The purpose of the present research is to recognize, specify and prioritize vital elements in the success of development centers by concentrating on the case study of the development center of Baqiyatallah University of Medical Sciences (BMSU).&lt;br /&gt; &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Primarily, In this regard, comprehensive literature review of more than 400 critical success indicators of parks and incubators were identified. Then, by integrating the overlays and the use of expert’s opinion, initial screening was conducted. The numbers were classified which were limited to 43 indicators in 5 clusters (5 elements). In this study, the Friedman test was used to rank the following factors and also the critical success subfactors of business incubator of BMSU.&lt;br /&gt; &lt;strong&gt;Results: &lt;/strong&gt;Findings indicate that factor of “human resources” with value of 4.19 among other factors and index of “supporting the commercialization of research results” as a part of “support and services of incubators” with value of 7.94 among other indexes, allocated the first ranks.&lt;br /&gt; &lt;strong&gt;Conclusions: &lt;/strong&gt;The outcome of this research, with the leading role of the Science and Technology Center of BMSU, was done in order to be used in strategic management and macro-policy making of the University.</Abstract>
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			<Object Type="keyword">
			<Param Name="value">science and technology park</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Business Incubator</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Critical success factors</Param>
			</Object>
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<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_75558_30f56d22e8afe413d9b7766f18b73ec4.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>5</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2018</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Investigating the Prevalence of Shigella Species and Their Antibiotic Resistance Pattern in Children With Acute Diarrhea Referred to Selected Hospitals in Tehran, Iran</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>70</FirstPage>
			<LastPage>74</LastPage>
			<ELocationID EIdType="pii">74245</ELocationID>
			
<ELocationID EIdType="doi">10.29252/jabr.05.02.06</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Peyman</FirstName>
					<LastName>Avakh Majalan</LastName>
<Affiliation>Biology Research Center, Faculty of Basic Sciences, Imam Hossain Comprehensive University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Abbas</FirstName>
					<LastName>Hajizade</LastName>
<Affiliation>Biology Research Center, Faculty of Basic Sciences, Imam Hossain Comprehensive University, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0003-3662-6681</Identifier>

</Author>
<Author>
					<FirstName>Shahram</FirstName>
					<LastName>Nazarian</LastName>
<Affiliation>Biology Research Center, Faculty of Basic Sciences, Imam Hossain Comprehensive University, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-4693-877X</Identifier>

</Author>
<Author>
					<FirstName>Mohammad Reza</FirstName>
					<LastName>Pourmand</LastName>
<Affiliation>Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Kiana</FirstName>
					<LastName>Amiri Siyavoshani</LastName>
<Affiliation>Department of Clinical Microbiology, Tehran University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2018</Year>
					<Month>03</Month>
					<Day>12</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;Introduction&lt;/strong&gt;: Shigellosis is a major health problem, especially in developing countries and in children under 5 years of age. The prevalence of &lt;em&gt;Shigella &lt;/em&gt;species in a region can be considered as an indicator for hygiene level of that region. Due to the lack of an efficient vaccine, antibiotic therapy is the main strategy to combat the disease. In this study, the prevalence of the &lt;em&gt;Shigella &lt;/em&gt;species and their antibiotic resistant pattern has been investigated.&lt;br /&gt; &lt;strong&gt;Materials and Methods: &lt;/strong&gt;A total of 300 diarrheal stool samples were collected from 4 different hospitals in Tehran during a period of 6 months June to November 2016. Bacterial identification and species discrimination was performed using biochemical and serotyping tests. Antibiotic resistance patterns of isolates were obtained using Bauer-Kirby method.&lt;br /&gt; &lt;strong&gt;Results: &lt;/strong&gt;8.7% of all diarrheal cases were caused by &lt;em&gt;Shigella &lt;/em&gt;species (5% by &lt;em&gt;Shigella sonnei &lt;/em&gt;and 3.7% by &lt;em&gt;Shigella flexneri&lt;/em&gt;). Antibiogram test revealed that the isolates were more sensitive or intermediate to ciprofloxacin (92.3%), while most of the isolates were resistant to tetracycline.&lt;br /&gt; &lt;strong&gt;Conclusions: &lt;/strong&gt;The prevalence of &lt;em&gt;Shigella &lt;/em&gt;species has changed in Tehran. Since antibiotics are the treatment of choice to combat these pathogens, also, because of the emergence of the antibiotic resistance &lt;em&gt;Shigella &lt;/em&gt;strains, there is a need for regularly updated regional antibiotic sensitivity patterns of the pathogen to guide therapy.</Abstract>
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			<Object Type="keyword">
			<Param Name="value">Shigella species</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Antibiotic Sensitivity Pattern</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Prevalence</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Diarrhea</Param>
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<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_74245_8491a034021d5b72964b56939d5f6239.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>5</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2018</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Construction and Sequencing of Dense Granular14 (GRA14) Gene of Toxoplasma gondii (RH) in Expression Prokaryotic Plasmid PET32a: A Preliminary Study in Vaccine Production</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>75</FirstPage>
			<LastPage>80</LastPage>
			<ELocationID EIdType="pii">74247</ELocationID>
			
<ELocationID EIdType="doi">10.29252/jabr.05.02.07</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Ashrafi</LastName>
<Affiliation>Department of Parasitology and Mycology, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Hossein</FirstName>
					<LastName>Sobati</LastName>
<Affiliation>Health Research Center, Life Style Institute, Baqiyatallah Universityof Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Seyyed Javad</FirstName>
					<LastName>Seyyed Tabaei</LastName>
<Affiliation>Department of Parasitology and Mycology, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2017</Year>
					<Month>12</Month>
					<Day>25</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;Introduction&lt;/strong&gt;: &lt;em&gt;Toxoplasma gondii &lt;/em&gt;is an obligatory intracellular protozoan parasite, which infects human beings. Since the current antigens used for diagnosis or vaccination are contaminated with non -parasitic material in which the parasite is grown, it is tried to produce recombinant antigens to design vaccines against toxoplasmosis, or make diagnostic kits. Choosing the type of antigen to produce recombinant vaccine or diagnostic kits is considerably important. The dense granule protein 14 (&lt;em&gt;GRA14&lt;/em&gt;) gene is one of the excretory-secretary antigens of &lt;em&gt;Toxoplasma &lt;/em&gt;which seems to be an appropriate candidate in production of recombinant vaccines and diagnostic kits. The current study aimed to clone &lt;em&gt;GRA14 &lt;/em&gt;gene of &lt;em&gt;T. gondii &lt;/em&gt;(RH) in a cloning vector for further production of dense granular proteins.&lt;br /&gt; &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Genomic DNA was isolated from tachyzoite of parasite by phenol chloroform method and gene fragment was amplified by polymerase chain reaction (PCR). The PCR products were ligated into restriction enzymes sites of pTG19-T cloning vector. Then transformed into &lt;em&gt;Escherichia coli &lt;/em&gt;Top10 strain and screened by IPTG and X-Gal. Then recombinant plasmid confirmed by the colony-PCR and restriction enzyme digestion using SacI and NotI was done followed by sequencing .After isolation of this gene from pTG19-T, it was subcloned into a prokaryotic expression plasmid (pET32a). The pET32a - GRA14 constructs were analyzed by PCR, restriction analysis and sequencing.&lt;br /&gt; &lt;strong&gt;Results: &lt;/strong&gt;Evaluation of PCR products by agarose gel electrophoresis and analysis of nucleotide sequencing of 1227 bp gene encoding the protein GRA14, revealed the complete homology with the recorded sequences in the gene bank. After enzyme restriction and electrophoresis a fragment about 1227 bp was separated from pET32a.&lt;br /&gt; &lt;strong&gt;Conclusions: &lt;/strong&gt;The result of this study showed that recombinant GRA14 &lt;em&gt;Toxoplasma &lt;/em&gt;was constructed successfully and ready for future study which seems like the antigen is a suitable candidate to produce recombinant vaccine and diagnostic kit.</Abstract>
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			<Object Type="keyword">
			<Param Name="value">Toxoplasma gondii</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Dense Granule Antigen 14</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cloning</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Subcloning</Param>
			</Object>
		</ObjectList>
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