RE: BD Sorter question

From: Robert Ashcroft, PhD (cytomat@netcore.com.au)
Date: Wed Mar 10 1999 - 07:37:25 EST


Gday again, Joseph.
This is one I can't resist!

Read that as "I can't remain psilent!"

The clock resolution of the drop delay is the relevant issue here.
In the MoFlo, it is 1/16th of a drop interval and in other machines, 1/10th
and as low as 1/4th .

The sorter knows where the cell is placed after measurement, within the
pertinent time resolution interval, 1/16th, 1/10th or 1/4th as the case may
be. One 1/16th is better than 1/4th , naturellement!

On MoFlo, a 1-2 mode of sorting will sort one drop 7/8th s of the time, but
when the target cell is known to be positioned in the first or last 1/16th
of the drop interval, a second drop is charged and sorted. A further
decision is involved according to whether enrich or purify mode is involved.
Enrich-mode ignores the contents of the adjacent drop, but purify-mode
defers to the contents of the adjacent drops, according to its pass/fail
contents.

In other machines, the process is called upon  more often than in MoFlo, so
they have more rejections of cells  as a result.
Bottom line: get better drop delay resolution: 1/16th > 1/10th > 1/4th .

I hope this helps.
We can talk about this, OK?

Pbob




-----Original Message-----
From:	Joseph Webster [mailto:J.Webster@centenary.usyd.edu.AU]
Sent:	Tuesday, 9 March 1999 12:58
To:	Cytometry Mailing List
Subject:	BD Sorter question


Hi All,
My head is not quite the right shape to get around some things...

Can someone please explain the algorithm or logic of partial-
drop sort decisions?
A couple of people have tried, but I have not understood yet...

One and three drop sort envelopes are understandable, but when I
tell the FACStar Plus to sort a two drop or a one-and-a-half drop
envelope, how does it choose which drops to collect?

Does it change between modes? (C, R, Counter, Enrich..)

	Thanks, Joseph.

--
Joseph Webster
Flow Cytometry Facility
Centenary Institute



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