Protocol tips
Upstream tips |
Protocol tips |
Downstream tips |
-Bring all reagents to room temperature before use.
-Do not include sodium azide in buffers or wash solutions if an HRP-labeled antibody/conjugate will
be used for detection. |
-Standards (duplicates or triplicates) and blank must be run with each plate to ensure
accuracy.
-Use a humidified incubator to reduce drying effects in the outside wells (“edge effects”) or place a wet tissue or blotter paper under the plates in non-humidified incubators.
-Do not stack plates.
|
|
Upstream tips |
-Bring all reagents to room temperature before use.
-Do not include sodium azide in buffers or wash solutions if an HRP-labeled antibody/conjugate will
be used for detection. |
Protocol tips |
-Standards (duplicates or triplicates) and blank must be run with each plate to ensure
accuracy.
-Use a humidified incubator to reduce drying effects in the outside wells (“edge effects”) or place a wet tissue or blotter paper under the plates in non-humidified incubators.
-Do not stack plates.
|
Publication protocol
The concentration of I-FABP was measured by Human I-FABP ELISA (Hycult Biotech, Uden, Netherlands), which is certified for both serum and urine. The assay was performed according to the manufacturer's instruction and the I-FABP concentration in serum is presented as ng/mL. To eliminate fluctuation in urine excretion, the urinary I-FABP was normalized to urinary creatinine and it is presented as pg/nmol of creatinine.
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