EFFECT OF PROTEINASE K AND ELUTION BUFFER ON DNA QUALITY OF PRIMARY SEX ORGANS OF KUNDHI BUFFALO

A study was conducted to optimize a rapid and cheaper mammalian DNA extraction protocol and to evaluate the effect of extracted DNA stored on various temperatures. Hundred fresh tissues of primary sex organs of Kundhi buffalo were collected from local slaughter house. The DNA was extracted using co...

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Main Authors: A. Ranjhani, P. Khatri, B. Bhutto, A. A. Memon, S. Mustafa
Format: Article
Language:English
Published: Sindh Agriculture University, Tandojam 2015-06-01
Series:Pakistan Journal of Agriculture, Agricultural Engineering & Veterinary Sciences
Subjects:
Online Access:https://pjaaevs.sau.edu.pk/index.php/ojs/article/view/145
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author A. Ranjhani
P. Khatri
B. Bhutto
A. A. Memon
S. Mustafa
author_facet A. Ranjhani
P. Khatri
B. Bhutto
A. A. Memon
S. Mustafa
author_sort A. Ranjhani
collection DOAJ
description A study was conducted to optimize a rapid and cheaper mammalian DNA extraction protocol and to evaluate the effect of extracted DNA stored on various temperatures. Hundred fresh tissues of primary sex organs of Kundhi buffalo were collected from local slaughter house. The DNA was extracted using commercial kit (protocol-1), its modified methods (protocol 2-4) and phenol chloroform method, the fresh and stored DNA was measured through spectrophotometer. The concentration of DNA extracted from ovary by using commercial kit and its modified methods of protocol 2, 3, 4 and phenol chloroform method  was 40.9, 42.2, 88.7, 226.2 and 232.7 ng/µl, respectively and with similar protocols in testes the concentration of extracted DNA was 41, 34.6, 64, 169.7 and 233.3 ng/µl, respectively. Significantly (P?0.001) higher concentration of DNA was obtained through modified methods of commercial kit and in phenol chloroform method than normal recommended protocol kit. The average purity (absorbance ratio A260/A280) from both primary sex organs was higher than 1.5 and ranged between 1.6-1.8 in ovary, whereas in testes it ranged between 1.6-2.0, in both of the organs. The higher absorbance ratio was measured through phenol chloroform method of DNA extraction. In conclusion the phenol chloroform and commercial kit methods yielded a good quality DNA and may be used for further experiments, like PCR related down streaming techniques. Phenol chloroform method is laborious but cost effective and may be used as an alternative of commercial kit for DNA extraction from primary sex organs of Kundhi buffalo.
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spelling doaj.art-64dc59b715be4e6cb27eb33120af8d362023-07-19T07:45:37ZengSindh Agriculture University, TandojamPakistan Journal of Agriculture, Agricultural Engineering & Veterinary Sciences1023-10722663-78632015-06-01311EFFECT OF PROTEINASE K AND ELUTION BUFFER ON DNA QUALITY OF PRIMARY SEX ORGANS OF KUNDHI BUFFALOA. Ranjhani0P. Khatri1B. Bhutto2A. A. Memon3S. Mustafa4Faculty of Animal Husbandry and Veterinary Sciences, Sindh Agriculture University Tandojam, PakistanFaculty of Animal Husbandry and Veterinary Sciences, Sindh Agriculture University Tandojam, PakistanFaculty of Animal Husbandry and Veterinary Sciences, Sindh Agriculture University Tandojam, PakistanFaculty of Animal Husbandry and Veterinary Sciences, Sindh Agriculture University Tandojam, PakistanFaculty of Animal Husbandry and Veterinary Sciences, Sindh Agriculture University Tandojam, Pakistan A study was conducted to optimize a rapid and cheaper mammalian DNA extraction protocol and to evaluate the effect of extracted DNA stored on various temperatures. Hundred fresh tissues of primary sex organs of Kundhi buffalo were collected from local slaughter house. The DNA was extracted using commercial kit (protocol-1), its modified methods (protocol 2-4) and phenol chloroform method, the fresh and stored DNA was measured through spectrophotometer. The concentration of DNA extracted from ovary by using commercial kit and its modified methods of protocol 2, 3, 4 and phenol chloroform method  was 40.9, 42.2, 88.7, 226.2 and 232.7 ng/µl, respectively and with similar protocols in testes the concentration of extracted DNA was 41, 34.6, 64, 169.7 and 233.3 ng/µl, respectively. Significantly (P?0.001) higher concentration of DNA was obtained through modified methods of commercial kit and in phenol chloroform method than normal recommended protocol kit. The average purity (absorbance ratio A260/A280) from both primary sex organs was higher than 1.5 and ranged between 1.6-1.8 in ovary, whereas in testes it ranged between 1.6-2.0, in both of the organs. The higher absorbance ratio was measured through phenol chloroform method of DNA extraction. In conclusion the phenol chloroform and commercial kit methods yielded a good quality DNA and may be used for further experiments, like PCR related down streaming techniques. Phenol chloroform method is laborious but cost effective and may be used as an alternative of commercial kit for DNA extraction from primary sex organs of Kundhi buffalo. https://pjaaevs.sau.edu.pk/index.php/ojs/article/view/145buffaloDNAporteinase Ktestes
spellingShingle A. Ranjhani
P. Khatri
B. Bhutto
A. A. Memon
S. Mustafa
EFFECT OF PROTEINASE K AND ELUTION BUFFER ON DNA QUALITY OF PRIMARY SEX ORGANS OF KUNDHI BUFFALO
Pakistan Journal of Agriculture, Agricultural Engineering & Veterinary Sciences
buffalo
DNA
porteinase K
testes
title EFFECT OF PROTEINASE K AND ELUTION BUFFER ON DNA QUALITY OF PRIMARY SEX ORGANS OF KUNDHI BUFFALO
title_full EFFECT OF PROTEINASE K AND ELUTION BUFFER ON DNA QUALITY OF PRIMARY SEX ORGANS OF KUNDHI BUFFALO
title_fullStr EFFECT OF PROTEINASE K AND ELUTION BUFFER ON DNA QUALITY OF PRIMARY SEX ORGANS OF KUNDHI BUFFALO
title_full_unstemmed EFFECT OF PROTEINASE K AND ELUTION BUFFER ON DNA QUALITY OF PRIMARY SEX ORGANS OF KUNDHI BUFFALO
title_short EFFECT OF PROTEINASE K AND ELUTION BUFFER ON DNA QUALITY OF PRIMARY SEX ORGANS OF KUNDHI BUFFALO
title_sort effect of proteinase k and elution buffer on dna quality of primary sex organs of kundhi buffalo
topic buffalo
DNA
porteinase K
testes
url https://pjaaevs.sau.edu.pk/index.php/ojs/article/view/145
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