Mapping The Genetic Diversity Of The Populations Of Cirrhinus Mrigala Through Mitochondrial Atpase 6/8 Genes From Indus Riverine System Of Pakistan (Record no. 8714)

000 -LEADER
fixed length control field 03126nam a22002057a 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20160711145708.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 160711b2016 xxu||||| |||| 00| 0 eng d
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title eng
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 2479-T
100 ## - MAIN ENTRY--AUTHOR NAME
Personal name Noor Muhammad (2014-VA-543)
110 ## - MAIN ENTRY--CORPORATE NAME
Location of meeting Dr. Fayyaz Rasool
245 ## - TITLE STATEMENT
Title Mapping The Genetic Diversity Of The Populations Of Cirrhinus Mrigala Through Mitochondrial Atpase 6/8 Genes From Indus Riverine System Of Pakistan
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Year of publication 2016.
300 ## - PHYSICAL DESCRIPTION
Number of Pages 79p.;
502 ## - DISSERTATION NOTE
Dissertation note This study was mapping the genetic diversity of Cirrhinus mrigala by using molecular markers for the ATPase 6/8 gene region. Samples of the target fish specie were collected from the different sites at the Indus riverine system of the Pakistan i.e Chenab (Head Qadirabad), Jhelum(Head Rasul), Ravi(Head Balloki) and Indus (Head Taunsa). Morphommetric parameters viz., Body weight, Girth, Total Length, Fork Length,Head length, Lengths of Caudal, Pectoral, Ventral Fins were recorded manually using measuring scale. After recording morphometric parameters blood from fish samples was drawn from caudal fin of the Fish, collected in Vautainer and immediately transferred into the Lab of IBBT where it is preserved in -80C for future use in DNA extraction. Phenol Chloroform Method of Genomic DNA extraction was used to extract whole blood DNA. The extracted DNA of the samples was run on 0.8% agarose gel by using electrophoresis of the DNA. Nanodrop was used to find out the concentration of DNA after that DNA was diluted according to the Need with deionized water. The PCR of ATPase 6/8 primers were used to amplify the target gene. The PCR product was confirm on 1.2% agarose gel. These gels were visualized in UV light and photographs were taken by Gel Documentation System (BIO-RAD, Gel-DOC EZ imager). After the visualizing of quality of band confirmation the samples were sent to be sequencing. The Analysis of Variance (ANOVA) for the different morphometric parameters was done by XLSTAT 2012 version 1.02. ANOVA results showed that all the morphomteric parameters were highly significant (p<0.01) within as well as between the groups. Pearson correlation analysis off overall population show that the body weight is positively correlated with the Fork Length, Total Length, Ventral Fin length, caudal Fin Length, Girth, with significant difference. Fork length is positively correlated with Total length, Ventral
Fin Length, Caudal Fin length, Pectoral Fin Length, with significant difference among other parameters. Total Length is positively correlated with Girth, Pectoral Fin Length, Ventral Fin Length, Caudal Fin Length, Girth, and Weight with significant difference among them. NJ methods suggested that existed relationship among different species located at different geographical locations. They all have a common ancestry. A strong relationship exists between fish species collected from different locations at Indus riverine system of Pakistan.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical Term Department of Zoology
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Mrs. Shakeela Parveen
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Dr. Muhammad Yasir Zahoor
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Thesis
Holdings
Damaged status Collection code Permanent Location Current Location Shelving location Date acquired Full call number Accession Number Koha item type
  Veterinary Science UVAS Library UVAS Library Thesis Section 2016-07-11 2479-T 2479-T Thesis


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