can we use a palindromic sequence having dsDNA labelled with cyanine fluorophores for fret experiments ?
Some things to think about:
Will the FRET donor and acceptor be close enough together for significant energy transfer to occur?
Will the DNA sequence have a tendency for a single strand to form a hairpin, which would compete with the formation of double-stranded DNA?
one strand - SSDNA - BIOTIN LABELLED another strand - SSDNA - NO LABEL without using NaCl , for Bli experiment ?
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How to Distinguish between DH5 alpha and BL21 cells if they are not labelled ?
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can you plese suggest other ways of restriction digestion of DNA.
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y = A1*exp(-x/t1) + A2*exp(-x/t2)+y0
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I have calculated the distance matrix in populations software. The data which i used is microsatellite data. I saved the distance matrix file in .txt format.But when I chose this same file to...
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After performing symmetric PCR, PCR purification was performed. Afterwards, asymmetric PCR was performed using the PCR purification product as a template, but no ssDNA band was confirmed in the...
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I have a Polyjet that has passed its labeled expiration date for 1 year and I'm going to re-start transfection experiments. It is really needed to change it? Transfection efficiency may be lower?
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The above are manually labeled extrinsic matrices based on the first image It can be seen that the projection error at the edge is large, while the error at the center is small. What could be the...
23 July 2024 7,479 3 View
We have mice brains that were over-fixed due to old PFA used during perfusion. Thus, the synapses are no longer being labeled by the Synaptophysin (SY38) mAB. which works perfectly every other...
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When preparing a graph of fluorophore intensity vs. analyte concentration, the linearity shows an R² of 0.999. However, when plotting the same data as Fo/F vs. analyte concentration, the linearity...
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Hello everyone. During my analyses on LC MSMS, the area ratio (Standard Area/Isotopically labelled Standard Area) increases with time for the quality control point. I'm having trouble explaining...
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How to store SDS-PAGE for fluorescent imaging without fixatives? I am running protein samples on SDS-PAGE that are tagged with fluorophores. If I place the gel in a destain solution of...
29 June 2024 8,720 1 View
I was performing quenching studies in solution state. While plotting the Stern-Volmer graph, which intensity should I use as initial intensity (I0). For example, I take 1 ml of 0.1 M fluorophore...
25 June 2024 5,385 1 View