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We are working on root-stock development of cultivated tomato by using Solanum lycopersicum and S. habrochaites. We would like to develop F1 of those species for using as root-stock. But S....
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In qPCR, we normally use 45 to 50 cycles of for getting good amplification curve. However, I have some primers which start to get amplification raising peak after 50 cycles and still not complete...
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We are working for developing markers in characterizing bolting time variations of cabbage lines, like early and late bolting time. We have tried to get PCR based polymorphism between them, in...
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We are making cross between tetraploid and diploid water melon, but in the seed mixture we found some selfed seeds, that might be fusion of diploid and haploid female gamets within the egg sac....
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In my qPCR, I have designed primers for 38 genes of Glucosinolate biosynthesis in cabbage. Where, my primers product sizes of those from 110 bp to 350 bp. However, in case of two genes, I have to...
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