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( A-C ) Quantification of neuron-specific enolase <t>(NSE)</t> levels in brain tissue lysate (A), blood plasma (B), and cerebrospinal fluid (CSF) (C) from wild-type (WT), Nrf2⁻/⁻, and ICAM-1⁻/⁻ mice under control and injury conditions (n = 8/group).( D-F ) Quantification <t>of</t> <t>S100β</t> levels in brain tissue lysate (D), blood plasma (E), and CSF (F) across the same experimental groups (n = 8/group). All values are expressed as mean ± SEM. Statistical analysis was performed using one-way ANOVA in A or two-way ANOVA in B and C followed by Dunnett’s post hoc test. Statistical significance between groups is indicated on the graphs. p < 0.05 statistically significant.
Neuron Specific Enolase Nse, supplied by Alpha Diagnostics, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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( A-C ) Quantification of neuron-specific enolase <t>(NSE)</t> levels in brain tissue lysate (A), blood plasma (B), and cerebrospinal fluid (CSF) (C) from wild-type (WT), Nrf2⁻/⁻, and ICAM-1⁻/⁻ mice under control and injury conditions (n = 8/group).( D-F ) Quantification <t>of</t> <t>S100β</t> levels in brain tissue lysate (D), blood plasma (E), and CSF (F) across the same experimental groups (n = 8/group). All values are expressed as mean ± SEM. Statistical analysis was performed using one-way ANOVA in A or two-way ANOVA in B and C followed by Dunnett’s post hoc test. Statistical significance between groups is indicated on the graphs. p < 0.05 statistically significant.
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( A-C ) Quantification of neuron-specific enolase <t>(NSE)</t> levels in brain tissue lysate (A), blood plasma (B), and cerebrospinal fluid (CSF) (C) from wild-type (WT), Nrf2⁻/⁻, and ICAM-1⁻/⁻ mice under control and injury conditions (n = 8/group).( D-F ) Quantification <t>of</t> <t>S100β</t> levels in brain tissue lysate (D), blood plasma (E), and CSF (F) across the same experimental groups (n = 8/group). All values are expressed as mean ± SEM. Statistical analysis was performed using one-way ANOVA in A or two-way ANOVA in B and C followed by Dunnett’s post hoc test. Statistical significance between groups is indicated on the graphs. p < 0.05 statistically significant.
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( A-C ) Quantification of neuron-specific enolase <t>(NSE)</t> levels in brain tissue lysate (A), blood plasma (B), and cerebrospinal fluid (CSF) (C) from wild-type (WT), Nrf2⁻/⁻, and ICAM-1⁻/⁻ mice under control and injury conditions (n = 8/group).( D-F ) Quantification <t>of</t> <t>S100β</t> levels in brain tissue lysate (D), blood plasma (E), and CSF (F) across the same experimental groups (n = 8/group). All values are expressed as mean ± SEM. Statistical analysis was performed using one-way ANOVA in A or two-way ANOVA in B and C followed by Dunnett’s post hoc test. Statistical significance between groups is indicated on the graphs. p < 0.05 statistically significant.
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( A-C ) Quantification of neuron-specific enolase <t>(NSE)</t> levels in brain tissue lysate (A), blood plasma (B), and cerebrospinal fluid (CSF) (C) from wild-type (WT), Nrf2⁻/⁻, and ICAM-1⁻/⁻ mice under control and injury conditions (n = 8/group).( D-F ) Quantification <t>of</t> <t>S100β</t> levels in brain tissue lysate (D), blood plasma (E), and CSF (F) across the same experimental groups (n = 8/group). All values are expressed as mean ± SEM. Statistical analysis was performed using one-way ANOVA in A or two-way ANOVA in B and C followed by Dunnett’s post hoc test. Statistical significance between groups is indicated on the graphs. p < 0.05 statistically significant.
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nse  (R&D Systems)
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( A-C ) Quantification of neuron-specific enolase <t>(NSE)</t> levels in brain tissue lysate (A), blood plasma (B), and cerebrospinal fluid (CSF) (C) from wild-type (WT), Nrf2⁻/⁻, and ICAM-1⁻/⁻ mice under control and injury conditions (n = 8/group).( D-F ) Quantification <t>of</t> <t>S100β</t> levels in brain tissue lysate (D), blood plasma (E), and CSF (F) across the same experimental groups (n = 8/group). All values are expressed as mean ± SEM. Statistical analysis was performed using one-way ANOVA in A or two-way ANOVA in B and C followed by Dunnett’s post hoc test. Statistical significance between groups is indicated on the graphs. p < 0.05 statistically significant.
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( A-C ) Quantification of neuron-specific enolase (NSE) levels in brain tissue lysate (A), blood plasma (B), and cerebrospinal fluid (CSF) (C) from wild-type (WT), Nrf2⁻/⁻, and ICAM-1⁻/⁻ mice under control and injury conditions (n = 8/group).( D-F ) Quantification of S100β levels in brain tissue lysate (D), blood plasma (E), and CSF (F) across the same experimental groups (n = 8/group). All values are expressed as mean ± SEM. Statistical analysis was performed using one-way ANOVA in A or two-way ANOVA in B and C followed by Dunnett’s post hoc test. Statistical significance between groups is indicated on the graphs. p < 0.05 statistically significant.

Journal: bioRxiv

Article Title: Nrf2 regulates ICAM-1–mediated neutrophil extracellular trap formation after traumatic brain injury

doi: 10.64898/2026.05.01.722360

Figure Lengend Snippet: ( A-C ) Quantification of neuron-specific enolase (NSE) levels in brain tissue lysate (A), blood plasma (B), and cerebrospinal fluid (CSF) (C) from wild-type (WT), Nrf2⁻/⁻, and ICAM-1⁻/⁻ mice under control and injury conditions (n = 8/group).( D-F ) Quantification of S100β levels in brain tissue lysate (D), blood plasma (E), and CSF (F) across the same experimental groups (n = 8/group). All values are expressed as mean ± SEM. Statistical analysis was performed using one-way ANOVA in A or two-way ANOVA in B and C followed by Dunnett’s post hoc test. Statistical significance between groups is indicated on the graphs. p < 0.05 statistically significant.

Article Snippet: Using commercial ELISA kits, the level of S100β (Abnova, Littleton CO, USA) and neuron specific enolase (NSE) (Alpha Diagnostic, San Antonio, Texas, USA; Cat. No 0050) were analyzed in tissue lysates as per manufacturer’s instructions.

Techniques: Clinical Proteomics, Control