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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Tehran University of Medical Sciences
2007-06-01
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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.
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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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