<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Parasitology">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>2</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2007</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Isolation of DNA from A Single Helminth Using New Developed Kit in Iran and Its PCR Analysis</title>
    <FirstPage>34</FirstPage>
    <LastPage>39</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>P Shayan</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>H Borji</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>A Eslami</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>S Zakeri</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Nematodes are among the most common and important parasites of man and animal. DNA of a single worm can be used for several purposes, such as identification to the species, subspecies, strain and antihelmenthic resistance.  DNA extraction from a single small worm using traditional methods such as phenol extraction technique faces serious prob&#xAC;lems. 
Methods: DNA from 20 single Haemonchus contortus   was isolated using DNA isolation kit newly designed in Iran by the Re&#xAC;search Unit of Molecular Biological System Transfer (MBST) based on the specific binding of DNA to the carrier. The ge&#xAC;nomic DNA was amplified using specific primers derived from &#x3B2;-tubulin isotype 1 in PCR. The specificity of the PCR prod&#xAC;ucts was determined using semi-nested PCR technique. Specific PCR-product from &#x3B2;-tubulin gene could be amplified with 1 ng, 100 pg and 10 pg DNA. 
Results: The used DNA extraction method was safe, with high quality and quantity, fast, easy to handle and not costly for ge&#xAC;netic analysis of even a single small worm. 
Conclusion: The Iran produced DNA extraction Kit is grounded on a selective binding of nucleic acids to a silica-based mem&#xAC;brane and is recommended for the isolation of DNA from even small amount of biological materials.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/23</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/23/22</pdf_url>
  </Article>
</Articles>
