http://confocal-microscopy-list.275.s1.nabble.com/How-to-show-something-inside-the-cell-tp7580451p7580463.html
Thank you for all valuable inputs. We can certainly try to quench the
fluorophore on the cell surface. However, I am wondering if the quencher
or incubated with the quenchers for too long. Some treatment seem quite
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> I can confirm Michaels comment below. During my research life, I was
> labelling bacteria with FITC, and observing uptake by cultured macrophages.
> Due to the conditions used, a lot of these FITC-bugs stuck to the outside
> of the cell, and I used Typan blue to quench the extracellular
> fluorescence. Details in
http://www.ncbi.nlm.nih.gov/pubmed/11726395>
> TITLE: Effects of surfactant protein A and NaCl concentration on the
> uptake of Pseudomonas aeruginosa by THP-1 cells. Khubchandani-Aswani KR,
> Oberley RE, Snyder JM.
>
> Cheers,
> Kavita
>
> Kavita Aswani, PhD
> Senior Applications Scientist - Life Sciences
> Lumen Dynamics Group Inc.
> 2260 Argentia Road, Mississauga, Ontario, Canada, L5N 6H7
> Direct Tel. 905 812-3342| Cell. 647 290 3506 * Toll Free (USA and Canada) 1
> 800 668-8752
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> -----Original Message-----
> From: Confocal Microscopy List [mailto:
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> On Behalf Of MODEL, MICHAEL
> Sent: June-07-13 7:04 AM
> To:
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> Subject: Re: How to show something inside the cell?
>
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> I think trypan blue has also been used to quench external fluorescence
> ________________________________________
> From: Confocal Microscopy List [
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> behalf of Gabriel Lapointe [
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> Sent: Thursday, June 06, 2013 5:17 PM
> To:
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> Subject: Re: How to show something inside the cell?
>
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> Hi Yi,
> In the same line of thougth as Mike, you could also look at the quencher
> used in qPCR. Some might be compatible with your fluorophore.
>
>
>
> *Gabriel Lapointe, M.Sc.*
> Lab Manager / Microscopy Specialist
> Concordia University, Biology Department
> 7141 Sherbrooke St. West SP 534
> Montréal QC H4B 1R6 Canada
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> 2013/6/6 MODEL, MICHAEL <
[hidden email]>
>
> > Hi Yi - I think your solution is good. Fluorophores on the surface can
> > also be selectively quenched, depending on the fluorophore - FITC by
> > lowering pH, red fluorophores or those emitting in the 600s by adding
> > several mg/ml of Acid Blue 9.
> >
> > Mike Model
> >
> >
> > -----Original Message-----
> > From: Confocal Microscopy List
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> > On Behalf Of SUBSCRIBE CONFOCALMICROSCOPY
> > Sent: Thursday, June 06, 2013 4:27 PM
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> > Subject: How to show something inside the cell?
> >
> > *****
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> >
> > Dear listers,
> >
> > One of our user is investigating the transportation of fluorescence
> > labeled DNA oligo in cells. He would like to prove the DNA oligo has
> > been transported inside the cells but not on the surface of cells by
> > using the light microscopy. We suggested him to clearly label the
> > membrane of cells and use the Z-stack images of confocal to look through
> the cells.
> > I am wondering if there is any other better solution?
> >
> > Any suggestion on good membrane dye is appreciated as well!
> >
> > Thank you,
> >
> > Yi
> >
> >
> >
>
> Think Green Before You Print!
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