نتایج جستجو برای: 171 dna bands were produced

تعداد نتایج: 4012914  

2015
Mohamed Said

A multiplex nested PCR technique was used to identify gender from single blastomeres biopsied from 8-cell mouse embryos. The primers amplified sequences of the Sry and Zfy genes on the Y-chromosome, and a polymorphic X chromosome microsatellite locus (DXNds-3). Amplification of male DNA gave three bands, of sizes 217 bp (Zfy), 147 bp (Sry) and 111 bp (Nds). In contrast, amplification of female ...

Journal: :journal of sciences, islamic republic of iran 2010
m. peyvandi

frequency of somaclonal variation in embryogenic calli and plants of olea europaea l cv.kroneiki derived from somatic embryogenesis were examined by randomly amplified polymorphic dna (rapd) analysis. radicle and cotyledon (proximal part) of mature zygotic embryo were cultured in omc medium supplemented with iba (5 mgl-1) and 2-ip (0.5 mgl-1). somatic embryogenesis was induced in calli of radic...

Journal: :Bionatura (Ibarra - Impresa) 2022

RAPD-PCR genetic markers were used to assess variation in wheat plants and connections among six genotypes. Four random primers produced 140 DNA fragments, averaging 6.7 identifiable bands per primer. Among the genotypes, 85 pieces (44.64 percent) polymorphic. Several RAPD marker had distinct signify recurrence patterns that thing differently amongst germplasm of groupings. Within-community acc...

Journal: :Cassowary 2021

Propagation through tissue culture by using orchid seed as explants will produce a lot of plants. This study aims to measure the genetic character plantlets that were regenerated from seeds which have been resulted in vitro culture. The original plants produced was determined Random Amplified Polymorphic DNA (RAPD) molecular markers. results showed primers used RAPD analysis polymorphic band pa...

Journal: :Nucleic acids research 1992
M F Riedy W J Hamilton C F Aquadro

The random amplified polymorphic DNA (RAPD) method allows the detection of DNA sequence polymorphisms using single primers of arbitrary sequence in the polymerase chain reaction (1). We have attempted to use this technique to assess paternity in a troop of chacma baboons {Papio cynocephalus ursinus). We have also examined individuals from known pedigrees of this species and humans. Our results ...

Journal: :caspian journal of environmental sciences 2014
al et m. gharibkhani

this study was conducted in order to investigate genetic diversity and population structure of pike-perch in the northern part of iran. for this purpose, 207 adult pike-perches from four regions of the caspian sea watershed (talesh coasts, anzali wetland, chaboksar coasts and aras dam) were collected. dna was extracted and by using 15 pairs of microsatellite primers, polymerase chain reaction (...

B Habibi-Khaniani , H Naghdi Badi , H Rassouli , K Baghalian , M Abdoli , S Shahnazi ,

  Background: Garlic is a valuable medicinal plant with variability in desirable morphological and physiological characteristics. The analysis of genetic diversity plays an important role in breeding programs. The RAPD technique could be very effective in detecting genetic variation in garlic.  Objective: The objective of the present work was to detect molecular polymorphism among Iranian garli...

2012
Niraj Tripathi Devendra Singh Chouhan Navinder Saini Sharad Tiwari

Genetic variations of 15 Brahmi (Bacopa monnieri L.) accessions were evaluated using random amplified polymorphic DNA (RAPD) and inter simple sequence repeats (ISSR) markers. During RAPD analysis, amplification of genomic DNA of the 15 accessions by 22 primers generated 197 fragments, of which 187 were polymorphic with an average of 8.95 bands per primer. The amplified products varied in size f...

اولادی, مرتضی, علوی, سید محمد, نعمت زاده, قربانعلی, هاشمی, سیدحمیدرضا ,

In three-line system, cytoplasmic male sterile (CMS) lines often were contaminated with cognate iso-nuclear maintainer lines during seeds multiplication processes. Therefore fingerprinting of breeding lines and identification of line-specific markers are prerequisite in genetic purity test. Six CMS lines including Neda-A, Nemat-A, Dasht-A, Amol 3-A, Champa-A, IR58025A and their iso-nuclear main...

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