Can you add a large excess of
non-fluorescent protein, such as BSA, to your solution to block the glass?
From:
Sent: Thursday, September 27, 2007
9:10 AM
To: [hidden email]
Subject: FCS of proteins in
solution
Dear all,
We are trying to perform fluorescence correlation
spectroscopy measurements on proteins in solution (PBS buffer). Our
sample is on a standard n0. 1.5 coverglass placed on an inverted
microscope. We are experiencing a lot of problems with adherence of the
proteins to the glass surface, in a sense that the signal is decreasing rapidly
after bringing the sample onto the glass. Is there a way to circumvent
this problem, eg by applying some coating to the coverglass or performing the
measurements in an other type of buffer?
Thanks for all suggestions,
Els
Dr. Ir. Els Vanstreels
Rega Institue for Medical Research
Minderbroedersstraat 10
3000 Leuven
Belgium
Tel.: +32-16332881
Fax.: +32-16332131
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