During a decolouration experiment for acidic dye, I noticed that the dye begin to degrade at higher pH values (using buffer solutions) without catalyst. Is this effect attributed to the buffer?
The deprotonated dyes are commonly oxidized by O2. This effect might be attributed to pH
Thanks Dr. Saeideh Hosseini, But I cannot upload the second paper.
www.ars.usda.gov/.../Place/.../Zhu170785_2004_Fluorescence.pdf
I couldn't found it.
I have reverse sequences (AB1 format), can I base on reverse DNA sequences to perform nucleotide alignment, convert nucleotides to amino acids and deposit the sequence in GenBank database?
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AI tools like ChatGPT can enhance research work significantly when used responsibly and in conjunction with thorough human oversight.
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Does anyone tried to do nucleofection with AMAXA by Lonza with lower than recommended amount of buffer in the cuvettes (100 ul)?
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Currently, when I run SDS-PAGE, I don't see any bands at all, even though I used the same material just a day ago and it worked fine.... In our lab, we dilute the 10X running buffer to 1X and...
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Hello everyone! How can i prepare EDTA buffer solution (pH 8.2) to determine GSH levels? Thank you in advance.
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// interested in the difference between floating events and short circuits.
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