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Irum Hasan's image  
Answer added by  Irum Hasan
6 years ago

Extract RNA Quantify its value (upto1 µg:1 ng-1 µg total RNA or pg- ng poly (A)-RNA) Put on ice immediately after incubation Add dNTPs (mM), nuclease-free water and the t ... See More

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Answer added by  Hadjer DAAS
7 years ago

on utilise des kittes d'extraction et de purification d'ADN afin d'ameleorer la technique d'amplification par PCR et ainsi southen blott 

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Answer added by  Vesna Mandusic , Research professor, Vinca Institute of Nuclear Sciences
7 years ago

In RNA sample (up to 1 µg :1 ng-1 µg total RNA or 50 pg-100 ng poly(A)-RNA Add primer oligo d(T) or  Random Primer(octamer or decamer). Incubate 5 min at 65 (for oligo dT ... See More

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Answer added by  sumera rashid
8 years ago

steps for cDNA synthesis: 1- isolate RNA 2- quantify its value for further reaction 3- prepare a reaction  containing;  oligo dT, water, RNA ample. 4- give it a heat shoc ... See More

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Answer added by  Esther Irungu, Waitress, Four Season Hotel Qatar
8 years ago

this are foods produced from organisms that have had changes introduced into their DNA using the methods of genetic engineering.

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Answer added by  Deleted user
8 years ago

genetically engineered foods are foods which have foreign genes inserted in their genetic codes to produce desired traits

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Answer added by  Maria Habib, Subject Matter Expert-Biology , Thomson Digital
8 years ago

By getting the random hexamer or oligo dt primers synthesized and setting up the PCR reaction using reverse transcriptase enzyme.