نتایج جستجو برای: pcr sscp

تعداد نتایج: 175795  

2004
M. R. BHIDE I. MIKULA

Tkáãiková a. , M. R. , Bhide I . Mikula: Asymmetric PCR-SSCP: a Useful Tool for Detection of OLA-DRB1(MHC class II) Gene Polymorphism in Slovak Improved Valachian Sheep. Acta Vet. Brno 2005, 74: 275-278. Detection of OLA-DBR1 (exon 2) gene polymorphism is presented in the paper. Rapid and inexpensive polymorphism detection method, namely, single stranded conformation polymorphism (SSCP) was ass...

2012
Elena Dehnavi Mojtaba Ahani Azari Saeed Hasani Mohammad Reza Nassiry Mokhtar Mohajer Alireza Khan Ahmadi Leila Shahmohamadi Soheil Yousefi

The aim of present study was to investigate myostatin gene polymorphism and its association with yearling weight records in Zel sheep using PCR-RFLP and PCR-SSCP methods. Blood samples were collected from 200 Zel sheep, randomly, and DNA was extracted using modified salting out method. Polymerase chain reaction was carried out to amplify 337, 222, and 311 bp fragments, respectively, comprising ...

Journal: :Genetics 1996
M F Antolin C F Bosio J Cotton W Sweeney M R Strand W C Black

The use of random amplified polymorphic DNA from the polymerase chain reaction (RAPD-PCR) allows efficient construction of saturated linkage maps. However, when analyzed by agarose gel electrophoresis, most RAPD-PCR markers segregate as dominant alleles, reducing the amount of linkage information obtained. We describe the use of single strand conformation polymorphism (SSCP) analysis of RAPD ma...

Journal: :research in pharmaceutical sciences 0

the sscp technique is based on the appearance of new “refolding” conformations during electro-phoresis due to mutation. in order to develop a simple, non-radioactive sscp analysis method so that it can reliably detect single nucleotide changes in pcr products up to 500 bp in length, extensive optimisation trials were performed . the best separation of sscp bands of pcr products up to 500 bp in ...

Journal: :BMC Infectious Diseases 2008
Subhash Chandra Parija Krishna Khairnar

BACKGROUND The level of intra-species genetic variation in Entamoeba histolytica, Entamoeba dispar and Entamoeba moshkovskii populations in a localized geographic area, like Puducherry, India, remains unknown. METHODS In the present study the existence of genetic variation in the nested multiplex polymerase chain reaction (NM-PCR) amplified region of the 16S-like ribosomal RNA genes of E. his...

Journal: :Environmental biosafety research 2007
Nicole Brinkmann Christoph C Tebbe

Cultivation-independent analyses were carried out to compare the bacterial community structure found in the rhizospheres of a transplastomic tobacco plant carrying the antibiotic resistance marker-gene aadA and its non-engineered parental line. PCR- and reverse transcriptase PCR-amplifications of 16S rRNA and their corresponding genes were carried out with primers targeting the domain Bacteria....

Journal: :Journal of clinical microbiology 2002
Tomotada Iwamoto Toshiaki Sonobe Kozaburo Hayashi

An algorithm to directly identify multiple mycobacterial species in a sample by using fluorescence capillary electrophoresis (FCE)-based single-strand conformation polymorphism (SSCP) analysis was developed. Part of the 16S-23S ribosomal DNA internal transcribed spacer (ITS) region in 37 reference strains and 73 clinical isolates representing 19 mycobacterial species and Mycobacterium tuberculo...

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2003
S B Jorge M B Melo F F Costa M F Sonati

Point mutations and small insertions or deletions in the human alpha-globin genes may produce alpha-chain structural variants and alpha-thalassemia. Mutations can be detected either by direct DNA sequencing or by screening methods, which select the mutated exon for sequencing. Although small (about 1 kb, 3 exons and 2 introns), the alpha-globin genes are duplicate (alpha2 and alpha1) and highly...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شهید چمران اهواز - دانشکده علوم 1391

روش بررسی: در این مطالعه ی توصیفی-آزمایشگاهی به شناسایی جهش در اگزون های 1، 2، 3، 5 و 8 ژن lrtomt در 157 بیمار پرداخته شد. dna از نمونه های خونی تمام بیماران به روش استاندارد فنل- کلروفرم استخراج شد. اگزون های مورد بررسی توسط واکنش زنجیره ای پلیمراز (pcr) تکثیر شدند. سپس جهش های ژن lrtomt با استفاده از روش pcr-sscp برای 5 اگزون، مورد بررسی قرار گرفتند. به علاوه، تمام نمونه ها بوسیله ی آنالیز ه...

ژورنال: :مجله دانشگاه علوم پزشکی شهرکرد 0
جواد صفاری چالشتری javad safarichaleshtori محمد تقی مرادی mohammad taghi moradi عفت فرخی efat farokhi محمد امین طباطبایی فر mohammadamin tabatabaee far مریم طاهر زاده m arym taherzadeh فاطمه شایسته fateme shayesteh غلامرضا مبینی

زمینه و هدف: سرطان معده دومین سرطان شایع در جهان است. فاکتورهای ژنتیکی مانند انکوژن ها و ژن های سرکوبگر تومور، همواره از جمله مهمترین عوامل در بروز این سرطان هستند. ژن p53 یک ژن سرکوبگر تومور است و نقش بسیار مهمی در فرآیند مرگ برنامه ریزی شده سلول ایفا می کند. جهش در ژن p53 موجب از بین رفتن عملکرد محافظتی آن شده که یکی ازعوامل اصلی بروز سرطان معده در انسان است. این مطالعه با هدف بررسی جهش های ژ...

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