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Direct Facs Protocol

1. Cells are stained with fluorescently labeled antibodies while on ice or at 4°C to prevent modulation and internalization of surface antigens. 2. Cells are incubated with primary labeled antibody for at least 30 minutes, then washed 3 times by centrifugation. 3. For short-term storage, cells can be kept on ice until analysis on the same day, but for longer storage cells should be fixed in 1% paraformaldehyde to prevent deterioration.

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Rafael Augusto Campos
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69 views1 page

Direct Facs Protocol

1. Cells are stained with fluorescently labeled antibodies while on ice or at 4°C to prevent modulation and internalization of surface antigens. 2. Cells are incubated with primary labeled antibody for at least 30 minutes, then washed 3 times by centrifugation. 3. For short-term storage, cells can be kept on ice until analysis on the same day, but for longer storage cells should be fixed in 1% paraformaldehyde to prevent deterioration.

Uploaded by

Rafael Augusto Campos
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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DIRECT STAINING PROTOCOL

(CELL SURFACE STAINING)

General Procedure:
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1.Harvest, wash the cells and adjust cell suspension to a concentration of 1-5x10 cells/ml in ice cold PBS,
10%FCS, 1%sodium azide* .

Cells are usually stained in polystyrene round-bottom 12x75 mm Falcon tubes. However, they can be stained in
any container for which you have an appropriate centrifuge e.g. test tubes, eppendorf tubes, and 96-well round-
bottomed microtiter plates. In general, cells should be spun down hard enough that the supernatant fluid can be
removed with little loss of cells, but not so hard that the cells are difficult to resuspend.
o
We recommend to stain with ice cold reagents/solutions and at 4 C as low temperature
and presence of sodium azide prevent the modulation and internalization of surface antigens
which can produce a loss of fluorescence intensity.

2. Add 0.1-10 µg/ml of the primary labelled antibody. Dilutions, if necessary, should be made in 3% BSA/PBS
(Propridium iodide can also be added at this point for dead cell exclusion).
o
3. Incubate for at least 30 min at room temperature or 4 C. This step will require optimisation.

4. Wash the cells 3X by centrifugation at 400 g for 5 minutes and resuspend them in 500ul to 1ml of ice cold PBS,
10% FCS,1% sodium azide*.

Keep the cells in the dark on ice or at 4oC in a fridge until your scheduled time for
analysis.

5. Analysis. For best results, analyze the cells on the flow cytometer as soon as possible.

We recommend analysis on the same day. For extended storage (16 hr) as well as for
greater flexibility in planning time on the cytometer, resuspend cells in 1%
paraformaldehyde to prevent deterioration

FIXATION:
If you need to wait longer than for an hour, you may need to fix the cells after step three. This can preserve them
for at least several days. (This will stabilize the light scatter and inactivate most biohazardous agents). Controls will
required fixation using the same procedure. Cells should not be fixed if they need to remain viable. There are
several methods available, please refer to fixation in the Indirect Staining protocol. The fixation for different
antigens will require optimisation by the user.

www.abcam.com/technical

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