I Have designed the Primers for MS-PCR and how to validate them. can we do the 5 gene methylation in a single tube? can anyone explain how to carry it out? practical approaches for MS-PCR and technical guidelines if any?
Thank you,
I am working in synthesis of material.
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Precision agriculture (PA), in India, is synonymous to Remote sensing, GIS, GPS, VRA and VRT. These are old technologies and during last 3-4 decades enough research has been carried out. But the...
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Just wants to know whether we can differentiate aerobic and anaerobic bacteria from same isolation method or we have to follow another method of estimation for anaerobic bacteria.
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During last 5-6 decades we have generated enough data from traditional experiments on nutrient management with graded levels of fertilizers in almost all systems and situations. Research on...
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Hi. Please tell me what guidelines should i need to follow for questionaries' type research work in India. It is not hospital based work, we are conduction basic institutional based qualitative...
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I have a dataset with about 80 different species. As usual, some species are very easy to identify with certainty whereas others are more difficult, which means that I am less certain of my...
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So, I have been trying to run a pACYC PCR which will be used later on for a Gibson Assembly. However the PCR is not working. I have already tried gradient PCR and changing extension time; however...
02 March 2021 1,146 2 View
I have to amplify a gene and my primers just reached. The Tm for Forward primer is 64.2, and that of reverse primer is 65.5. Can some one suggest how to get the best annealing temperature? Thanks...
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I am trying to identify these 3 genes among some tomato cultivar collections and after aligning some sequences from NCBI, I couldn't find unique sequences to target for specific primers. There...
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hello everyone, I need to do standard curves for my qPCR, what is the ideal efficiency range? I tried a primer (Mglu2 receptor) that gave an efficiency of 90.2%. Is it accepted?
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Dear All, mirna primer showing some problem in the melting curve? any idea why? As attached is the melting curve. The forward sequence is obtained from miRBase and reverse primer is universal.
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Hi I am a bit confused. They are asking me to find out the volume of DNA required in ul (a total of 30-100 ng for genomic DNA) from the DNA concentration in the nanodrop reading which was 404.8...
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Hi everyone, Illumina provides a list of primers to amplify with high taxonomic coverage the ITS1 region for further fungal sequencing, but I cannot find the exact amount necessary of each...
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