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| ID | Components | Size |
| RSP002-C01 | Pre-coated Anti-IFN-γ Antibody Microplate | 1 plate |
| RSP002-C02 | Positive Stimulus | 60 μg |
| RSP002-C03 | Biotin-Anti-IFN-γ Antibody | 50 μL |
| RSP002-C04 | Streptavidin-HRP | 50 μL |
| RSP002-C05 | Washing Buffer (10x) | 50 mL |
| RSP002-C06 | Dilution Buffer (1x) | 50 mL |
| RSP002-C07 | AEC Dilution | 25 mL |
| RSP002-C08 | AEC Solution A (20x) | 0.8 mL |
| RSP002-C09 | AEC Solution B (20x) | 0.8 mL |
| RSP002-C10 | AEC Solution C (20x) | 0.8 mL |
This kit is used to detect IFN-γ at the cellular level.
It is for research use only.
2. Find the expiration date on the outside packaging and do not use reagents past their expiration date.
3. Please use it up once you opened it.
Your experiment will include 6 simple steps:
a) A monoclonal antibody specific for mouse IFN-γ has been pre-coated onto a polyvinylidene difluoride (PVDF)-backed microplate.
b) Appropriately stimulated cells are pipetted into the wells and the microplate is placed into a humidified 37 °C CO2 incubator for a specified period of time.During this incubation period, the immobilized antibody in the immediate vicinity of the secreting cells binds secreted IFN-γ.
c) After washing away any cells and unbound substances, a biotinylated antibody specific for mouse IFN-γ is added to the wells. Following a wash to remove any unbound biotinylated antibody, HRP conjugated to streptavidin is added.
d) Wash the plate and add the Streptavidin-HRP diluted by Dilution Buffer to the plate.
e) Wash the plate and add AEC. A reddish-brown colored precipitate forms and appears as spots at the sites of cytokine localization, with each individual spot representing an individual IFN-γ secreting cell.
f) The spots can be counted with an automated ELISpot reader system or manually using a stereomicroscope.
1x10⁵ cells/well Mouse Spleen Cells were stimulated with 6.0 μg/mL ConA and cultured at 37℃ and 5%CO2 for 20h, 308 spots were produced. The following example data is for reference only.
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