Protocol tips
Upstream tips |
Protocol tips |
Downstream tips |
-Equilibrate all reagents to room temperature (18-25°C) prior to use. |
-Avoid foaming or bubbles when mixing or reconstituting components.
-Ensure plates are properly sealed or covered during incubation steps.
-Complete removal of all solutions and buffers during wash steps is necessary to minimize background. |
-Unused well strips should be returned to the plate packet and
stored at 4°C. |
Upstream tips |
-Equilibrate all reagents to room temperature (18-25°C) prior to use. |
Protocol tips |
-Avoid foaming or bubbles when mixing or reconstituting components.
-Ensure plates are properly sealed or covered during incubation steps.
-Complete removal of all solutions and buffers during wash steps is necessary to minimize background. |
Downstream tips |
-Unused well strips should be returned to the plate packet and
stored at 4°C. |
Publication protocol
Immediately after culling, blood was collected from n≥8 control and Foxg1Cre/+; ARfl/y mice by cardiac puncture with a syringe and needle pre-treated with heparin. Plasma was separated by centrifugation and stored at-80. Testosterone was measured using a radioimmunoassay as previously described [24]. LH and FSH were measured using in-house designed ELISAs as previously described [25]. Commercially available ELISAs for prolactin (Abcam #ab100736), GH (Merck Millipore EZRMGH-45K), ACTH (Antibodies Online #ABIN415571) and TSH (Antibodies Online #ABIN415519) were performed according to manufacturer’s instructions. All samples were run in duplicate in a single assay for each hormone.
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