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Detection of Th17 (3-color) in Mouse Spleen

Source: Elabscience®Published: Dec 21,2023

             

Purpose

Sample

Antibody Collocation

Adjust the voltage

1

Blank

Adjust compensation

2

CD3-PerCP/Cyanine5.5

3

CD4-FITC

4

IL-17A-PE

PE-FMO in combination with Isotype Control for auxiliary gating

5

CD3-PerCP/Cyanine5.5, CD4-FITC, Rat IgG1, κ Isotype Control-PE

Full panel

6

CD3-PerCP/Cyanine5.5, CD4-FITC, IL-17A-PE

Marker

Fluorochrome

Clone No.

Cat. No.

CD3

PerCP/Cyanine5.5

17A2

E-AB-F1013J

CD4

FITC

RM4-5

E-AB-F1353C

IL-17A

PE

TC11-18H10.1

E-AB-F1199D

Rat IgG1,κ Isotype Control

PE

HRPN

E-AB-F09822D

 
Detection of Th17 (3-color) in Mouse Spleen-1
 

Tips:

1. After the preparation and counting of the splenic single-cell suspension are completed, it is necessary to perform stimulation and inhibition culture using cytokine stimulation inhibitors (for experimental conditions of stimulation and inhibition, please refer to the instructions of the reagent kit used).

2. PMA stimulation can induce partial internalization of CD4 on the surface of human T cells. Therefore, it is necessary to select the CD4 clone RM4-5, which has minimal impact on internalization.

3. Isotype controls are required for IL-17A because cytokine expression levels are generally low.

4. Th17 cells are characterized by the CD3⁺CD4⁺IL-17A⁺ phenotype.

5. Permeabilization reagents can cause significant damage to cells. It is recommended to first resuspend the cell pellet into a single-cell suspension after centrifugation before adding the permeabilization reagent, in order to minimize cell loss.