Protocol tips
Upstream tips |
Protocol tips |
Downstream tips |
-Store the unopened kit at 2-8 °C.
-Bring all reagents to room temperature before use.
-Reconstitute the Human Cytochrome c Standard with deionized or distilled water. Allow the standard to sit for a minimum of 15 minutes with gentle agitation prior to making dilutions. |
-When mixing or reconstituting protein solutions, always avoid foaming.
-Substrate Solution should remain colorless until added to the plate.
-Keep Substrate solution protected from light.
-Stop Solution should be added to the plate in the same order as the Substrate Solution.
-Wells that are green in color indicate that the Stop Solution has not mixed thoroughly with
the Substrate Solution. |
|
Upstream tips |
-Store the unopened kit at 2-8 °C.
-Bring all reagents to room temperature before use.
-Reconstitute the Human Cytochrome c Standard with deionized or distilled water. Allow the standard to sit for a minimum of 15 minutes with gentle agitation prior to making dilutions. |
Protocol tips |
-When mixing or reconstituting protein solutions, always avoid foaming.
-Substrate Solution should remain colorless until added to the plate.
-Keep Substrate solution protected from light.
-Stop Solution should be added to the plate in the same order as the Substrate Solution.
-Wells that are green in color indicate that the Stop Solution has not mixed thoroughly with
the Substrate Solution. |
Publication protocol
The concentrations of studied parameters in serum samples were measured by the enzyme-linked immunosorbent assay (ELISA) using commercially available kits according to manufacturer’s detailed instructions: for Tumor Necrosis Factor alpha (TNF-α)—Quantikine ELISA Human TNF-α kit, for Fas—Quantikine ELISA Human Fas/TNFRSF6 kit, for Fas Ligand (FasL)—Quantikine ELISA Human Fas Ligand/TNFSF6 kit, for soluble TNF receptor I (sTNF RI)—Quantikine ELISA Human sTNF RI/TNFRSF1A kit and for soluble TNF receptor II (sTNF RII)—Quantikine ELISA Human TNF RII/TNFRSF1B kit (all kits from R&D Systems, MN, USA). The coefficients of variance for intra-assay and inter-assay were below 8% and 10%, respectively.
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