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Densitometric analysis of PSD95, <t>SYT,</t> <t>and</t> <t>SYP</t> protein levels of CTRL and BPA‐treated cells. The level of ACTIN protein was used as a loading control for protein normalization in western blot analysis. For both CTRL and BPA‐treated samples, each lane represents an independent biological replicate of the experiment. Values are reported as mean ± SEM. * p ≤ 0.05, ** p ≤ 0.01. Uncropped gels are provided in the Figure .
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Densitometric analysis of PSD95, SYT, and SYP protein levels of CTRL and BPA‐treated cells. The level of ACTIN protein was used as a loading control for protein normalization in western blot analysis. For both CTRL and BPA‐treated samples, each lane represents an independent biological replicate of the experiment. Values are reported as mean ± SEM. * p ≤ 0.05, ** p ≤ 0.01. Uncropped gels are provided in the Figure .

Journal: Journal of Biochemical and Molecular Toxicology

Article Title: Bisphenol A Treatment Impairs Synaptic Function in Human Cholinergic Neurons

doi: 10.1002/jbt.70558

Figure Lengend Snippet: Densitometric analysis of PSD95, SYT, and SYP protein levels of CTRL and BPA‐treated cells. The level of ACTIN protein was used as a loading control for protein normalization in western blot analysis. For both CTRL and BPA‐treated samples, each lane represents an independent biological replicate of the experiment. Values are reported as mean ± SEM. * p ≤ 0.05, ** p ≤ 0.01. Uncropped gels are provided in the Figure .

Article Snippet: Following blocking, the membranes were incubated overnight, at 4°C with primary antibodies against SYP (AB9272; Merk‐Millipore; dilution 1:80,000), SYT (#14558; Cell Signaling Technology; dilution 1:1000), PSD‐95 (#2507; Cell Signaling Technology; dilution 1:1000), PARP‐1 (AB‐83632; Immunological Science; dilution 1:1000), and CASP‐3 (sc‐271028; Santa Cruz; dilution 1:1000).

Techniques: Control, Western Blot