Isolation of DNA from A Single Helminth Using New Developed Kit in Iran and Its PCR Analysis

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 method...

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Main Authors: P Shayan, H Borji, A Eslami, S Zakeri
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2007-06-01
Series:Iranian Journal of Parasitology
Subjects:
Online Access:https://ijpa.tums.ac.ir/index.php/ijpa/article/view/23
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spelling doaj-4816240b1cee45c1a922981e69dd29512021-04-02T11:45:41ZengTehran University of Medical SciencesIranian Journal of Parasitology1735-70202008-238X2007-06-0122Isolation of DNA from A Single Helminth Using New Developed Kit in Iran and Its PCR Analysis P Shayan0 H Borji1 A Eslami2 S Zakeri3 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¬lems. Methods: DNA from 20 single Haemonchus contortus was isolated using DNA isolation kit newly designed in Iran by the Re¬search Unit of Molecular Biological System Transfer (MBST) based on the specific binding of DNA to the carrier. The ge¬nomic DNA was amplified using specific primers derived from β-tubulin isotype 1 in PCR. The specificity of the PCR prod¬ucts was determined using semi-nested PCR technique. Specific PCR-product from β-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¬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¬brane and is recommended for the isolation of DNA from even small amount of biological materials. https://ijpa.tums.ac.ir/index.php/ijpa/article/view/23Genomic DNASemi-nested PCR
collection DOAJ
language English
format Article
sources DOAJ
author P Shayan
H Borji
A Eslami
S Zakeri
spellingShingle P Shayan
H Borji
A Eslami
S Zakeri
Isolation of DNA from A Single Helminth Using New Developed Kit in Iran and Its PCR Analysis
Iranian Journal of Parasitology
Genomic DNA
Semi-nested PCR
author_facet P Shayan
H Borji
A Eslami
S Zakeri
author_sort P Shayan
title Isolation of DNA from A Single Helminth Using New Developed Kit in Iran and Its PCR Analysis
title_short Isolation of DNA from A Single Helminth Using New Developed Kit in Iran and Its PCR Analysis
title_full Isolation of DNA from A Single Helminth Using New Developed Kit in Iran and Its PCR Analysis
title_fullStr Isolation of DNA from A Single Helminth Using New Developed Kit in Iran and Its PCR Analysis
title_full_unstemmed Isolation of DNA from A Single Helminth Using New Developed Kit in Iran and Its PCR Analysis
title_sort isolation of dna from a single helminth using new developed kit in iran and its pcr analysis
publisher Tehran University of Medical Sciences
series Iranian Journal of Parasitology
issn 1735-7020
2008-238X
publishDate 2007-06-01
description 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¬lems. Methods: DNA from 20 single Haemonchus contortus was isolated using DNA isolation kit newly designed in Iran by the Re¬search Unit of Molecular Biological System Transfer (MBST) based on the specific binding of DNA to the carrier. The ge¬nomic DNA was amplified using specific primers derived from β-tubulin isotype 1 in PCR. The specificity of the PCR prod¬ucts was determined using semi-nested PCR technique. Specific PCR-product from β-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¬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¬brane and is recommended for the isolation of DNA from even small amount of biological materials.
topic Genomic DNA
Semi-nested PCR
url https://ijpa.tums.ac.ir/index.php/ijpa/article/view/23
work_keys_str_mv AT pshayan isolationofdnafromasinglehelminthusingnewdevelopedkitinirananditspcranalysis
AT hborji isolationofdnafromasinglehelminthusingnewdevelopedkitinirananditspcranalysis
AT aeslami isolationofdnafromasinglehelminthusingnewdevelopedkitinirananditspcranalysis
AT szakeri isolationofdnafromasinglehelminthusingnewdevelopedkitinirananditspcranalysis
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