bs-3220R Search Results


94
Bioss rabbit anti p erbb4 antibody
<t>ErbB4</t> small molecule agonist ameliorates cognitive behavioral impairments in mice exposed to PS-MPs. ( A ) Representative traces in open field experiment. ( B ) The statistical analysis related to open field test. ( C ) Representative heat map in Y maze exploration experiment, with arm A denoting the initial arm. ( D ) The rate of spontaneous alternation in Y maze experiment. ( E ) Representative traces from the new object recognition (NOR) experiment. ( F ) Statistical analysis related to the NOR experiment. ( G ) Representative swimming traces from the Morris water maze (MWM) exploration experiment. ( H ) The statistical analysis of MWM exploration test. Statistical analysis was conducted using one-way analysis of variance (ANOVA) followed by Tukey’s post hoc test for multiple comparisons, and the data are presented as means ± standard error of the mean (SEM). Statistical significance is indicated by * p < 0.05, ** p < 0.01, and *** p < 0.001, with n = 8 per group
Rabbit Anti P Erbb4 Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ErbB4 small molecule agonist ameliorates cognitive behavioral impairments in mice exposed to PS-MPs. ( A ) Representative traces in open field experiment. ( B ) The statistical analysis related to open field test. ( C ) Representative heat map in Y maze exploration experiment, with arm A denoting the initial arm. ( D ) The rate of spontaneous alternation in Y maze experiment. ( E ) Representative traces from the new object recognition (NOR) experiment. ( F ) Statistical analysis related to the NOR experiment. ( G ) Representative swimming traces from the Morris water maze (MWM) exploration experiment. ( H ) The statistical analysis of MWM exploration test. Statistical analysis was conducted using one-way analysis of variance (ANOVA) followed by Tukey’s post hoc test for multiple comparisons, and the data are presented as means ± standard error of the mean (SEM). Statistical significance is indicated by * p < 0.05, ** p < 0.01, and *** p < 0.001, with n = 8 per group

Journal: Journal of Neuroinflammation

Article Title: Targeted activation of ErbB4 receptor ameliorates neuronal deficits and neuroinflammation in a food-borne polystyrene microplastic exposed mouse model

doi: 10.1186/s12974-025-03406-6

Figure Lengend Snippet: ErbB4 small molecule agonist ameliorates cognitive behavioral impairments in mice exposed to PS-MPs. ( A ) Representative traces in open field experiment. ( B ) The statistical analysis related to open field test. ( C ) Representative heat map in Y maze exploration experiment, with arm A denoting the initial arm. ( D ) The rate of spontaneous alternation in Y maze experiment. ( E ) Representative traces from the new object recognition (NOR) experiment. ( F ) Statistical analysis related to the NOR experiment. ( G ) Representative swimming traces from the Morris water maze (MWM) exploration experiment. ( H ) The statistical analysis of MWM exploration test. Statistical analysis was conducted using one-way analysis of variance (ANOVA) followed by Tukey’s post hoc test for multiple comparisons, and the data are presented as means ± standard error of the mean (SEM). Statistical significance is indicated by * p < 0.05, ** p < 0.01, and *** p < 0.001, with n = 8 per group

Article Snippet: Specifically, the sections were treated with a mouse anti-β3-tubulin antibody (1:100, sc80016, Santa Cruz Biotechnology, USA) in combination with one of the following antibodies: rabbit anti-p-ErbB4 antibody (1:200, bs-3220R, Bioss, Beijing, China), and rabbit anti-synaptophysin (SYP) antibody (1:200, AF8091, Beyotime, Shanghai, China).

Techniques:

ErbB4 small molecule agonist can improve the dendritic spine injury of hippocampal neurons in mice exposed to PS-MPs. ( A ) Representative images of neuronal dendritic segments. scale bar, 10 μm. ( B ) Total dendritic spine density of hippocampal neurons. ( C ) The density of mushroom spines in hippocampal neurons. Statistical analysis was conducted using one-way ANOVA followed by Tukey’s post hoc test for multiple comparisons.The results were presented as means ± SEM. Statistical significance is indicated by * p < 0.05, ** p < 0.01, and *** p < 0.001, with n = 4 per group

Journal: Journal of Neuroinflammation

Article Title: Targeted activation of ErbB4 receptor ameliorates neuronal deficits and neuroinflammation in a food-borne polystyrene microplastic exposed mouse model

doi: 10.1186/s12974-025-03406-6

Figure Lengend Snippet: ErbB4 small molecule agonist can improve the dendritic spine injury of hippocampal neurons in mice exposed to PS-MPs. ( A ) Representative images of neuronal dendritic segments. scale bar, 10 μm. ( B ) Total dendritic spine density of hippocampal neurons. ( C ) The density of mushroom spines in hippocampal neurons. Statistical analysis was conducted using one-way ANOVA followed by Tukey’s post hoc test for multiple comparisons.The results were presented as means ± SEM. Statistical significance is indicated by * p < 0.05, ** p < 0.01, and *** p < 0.001, with n = 4 per group

Article Snippet: Specifically, the sections were treated with a mouse anti-β3-tubulin antibody (1:100, sc80016, Santa Cruz Biotechnology, USA) in combination with one of the following antibodies: rabbit anti-p-ErbB4 antibody (1:200, bs-3220R, Bioss, Beijing, China), and rabbit anti-synaptophysin (SYP) antibody (1:200, AF8091, Beyotime, Shanghai, China).

Techniques:

ErbB4 small molecule agonist can improve synaptic dysfunction of hippocampal neurons in mice exposed to PS-MPs. ( A ) The ultrastructural analysis of hippocampal neuron synapses was performed using transmission electron microscopy (TEM). ( B ) Statistical analyses were conducted on the synaptic data of hippocampal neurons. ( C ) Immunofluorescence was employed to detect the levels of synaptophysin (SYP) and β3-tubulin. ( D ) Western blot analysis was utilized to assess the protein levels of synapse-associated proteins, including DOCK3, p-CREB, CREB, SYP, GAP43, PSD95, and SYT1 in hippocampal neurons. ( E ) Statistical analyses of these protein levels were performed using one-way ANOVA with Tukey’s multiple comparison test. The synaptic structure was examined at a magnification of 10,000×, with a scale bar of 1 μm. Results are expressed as means ± SEM. Immunofluorescence labeling was as follows: SYP in red and β3-tubulin in green, with a scale bar of 20 μm. Statistical significance was indicated by * p < 0.05, ** p < 0.01, and *** p < 0.001, with a sample size of n = 4 per group

Journal: Journal of Neuroinflammation

Article Title: Targeted activation of ErbB4 receptor ameliorates neuronal deficits and neuroinflammation in a food-borne polystyrene microplastic exposed mouse model

doi: 10.1186/s12974-025-03406-6

Figure Lengend Snippet: ErbB4 small molecule agonist can improve synaptic dysfunction of hippocampal neurons in mice exposed to PS-MPs. ( A ) The ultrastructural analysis of hippocampal neuron synapses was performed using transmission electron microscopy (TEM). ( B ) Statistical analyses were conducted on the synaptic data of hippocampal neurons. ( C ) Immunofluorescence was employed to detect the levels of synaptophysin (SYP) and β3-tubulin. ( D ) Western blot analysis was utilized to assess the protein levels of synapse-associated proteins, including DOCK3, p-CREB, CREB, SYP, GAP43, PSD95, and SYT1 in hippocampal neurons. ( E ) Statistical analyses of these protein levels were performed using one-way ANOVA with Tukey’s multiple comparison test. The synaptic structure was examined at a magnification of 10,000×, with a scale bar of 1 μm. Results are expressed as means ± SEM. Immunofluorescence labeling was as follows: SYP in red and β3-tubulin in green, with a scale bar of 20 μm. Statistical significance was indicated by * p < 0.05, ** p < 0.01, and *** p < 0.001, with a sample size of n = 4 per group

Article Snippet: Specifically, the sections were treated with a mouse anti-β3-tubulin antibody (1:100, sc80016, Santa Cruz Biotechnology, USA) in combination with one of the following antibodies: rabbit anti-p-ErbB4 antibody (1:200, bs-3220R, Bioss, Beijing, China), and rabbit anti-synaptophysin (SYP) antibody (1:200, AF8091, Beyotime, Shanghai, China).

Techniques: Transmission Assay, Electron Microscopy, Immunofluorescence, Western Blot, Comparison, Labeling

ErbB4 small molecule agonist can improve mitochondrial damage in hippocampal neurons of mice exposed to PS-MPs. ( A ) The ultrastructural integrity of hippocampal neuronal mitochondria was evaluated using transmission electron microscopy (TEM). ( B ) Statistical analyses were performed on data pertaining to the hippocampal neuronal mitochondria. ( C ) The expression levels of mitochondria-associated proteins, including phosphorylated mTOR (p-mTOR), mTOR, and SIRT3, in the hippocampus of mice were quantified via western blot analysis. ( D ) Statistical analyses of these protein expression levels were conducted using one-way ANOVA followed by Tukey’s post hoc test for multiple comparisons. The original magnification for mitochondrial imaging was 2000×, with a scale bar of 5 μm. Data are presented as means ± SEM. Statistical significance was indicated by * p < 0.05, ** p < 0.01, and *** p < 0.001, with a sample size of n = 4 per group

Journal: Journal of Neuroinflammation

Article Title: Targeted activation of ErbB4 receptor ameliorates neuronal deficits and neuroinflammation in a food-borne polystyrene microplastic exposed mouse model

doi: 10.1186/s12974-025-03406-6

Figure Lengend Snippet: ErbB4 small molecule agonist can improve mitochondrial damage in hippocampal neurons of mice exposed to PS-MPs. ( A ) The ultrastructural integrity of hippocampal neuronal mitochondria was evaluated using transmission electron microscopy (TEM). ( B ) Statistical analyses were performed on data pertaining to the hippocampal neuronal mitochondria. ( C ) The expression levels of mitochondria-associated proteins, including phosphorylated mTOR (p-mTOR), mTOR, and SIRT3, in the hippocampus of mice were quantified via western blot analysis. ( D ) Statistical analyses of these protein expression levels were conducted using one-way ANOVA followed by Tukey’s post hoc test for multiple comparisons. The original magnification for mitochondrial imaging was 2000×, with a scale bar of 5 μm. Data are presented as means ± SEM. Statistical significance was indicated by * p < 0.05, ** p < 0.01, and *** p < 0.001, with a sample size of n = 4 per group

Article Snippet: Specifically, the sections were treated with a mouse anti-β3-tubulin antibody (1:100, sc80016, Santa Cruz Biotechnology, USA) in combination with one of the following antibodies: rabbit anti-p-ErbB4 antibody (1:200, bs-3220R, Bioss, Beijing, China), and rabbit anti-synaptophysin (SYP) antibody (1:200, AF8091, Beyotime, Shanghai, China).

Techniques: Transmission Assay, Electron Microscopy, Expressing, Western Blot, Imaging

ErbB4 small molecule agonist enhances the ErbB4 signaling pathway in hippocampus of mice exposed to PS-MPs. ( A ) Immunofluorescence was used to detect levels of phosphorylated ErbB4 (p-ErbB4) and β3-tubulin. ( B ) Protein levels associated with the ErbB4 signaling pathway in the hippocampus of mice were assessed through western blot analysis. ( C ) A statistical analysis was performed on the data derived from protein levels, employing one-way ANOVA with Tukey’s multiple comparison tests. The p-ErbB4 is represented in red, while β3-tubulin is depicted in green, with a scale bar of 20 μm. The results are expressed as means ± SEM, with significance levels indicated by * p < 0.05, ** p < 0.01, and *** p < 0.001. Each experimental group comprised n = 4 samples

Journal: Journal of Neuroinflammation

Article Title: Targeted activation of ErbB4 receptor ameliorates neuronal deficits and neuroinflammation in a food-borne polystyrene microplastic exposed mouse model

doi: 10.1186/s12974-025-03406-6

Figure Lengend Snippet: ErbB4 small molecule agonist enhances the ErbB4 signaling pathway in hippocampus of mice exposed to PS-MPs. ( A ) Immunofluorescence was used to detect levels of phosphorylated ErbB4 (p-ErbB4) and β3-tubulin. ( B ) Protein levels associated with the ErbB4 signaling pathway in the hippocampus of mice were assessed through western blot analysis. ( C ) A statistical analysis was performed on the data derived from protein levels, employing one-way ANOVA with Tukey’s multiple comparison tests. The p-ErbB4 is represented in red, while β3-tubulin is depicted in green, with a scale bar of 20 μm. The results are expressed as means ± SEM, with significance levels indicated by * p < 0.05, ** p < 0.01, and *** p < 0.001. Each experimental group comprised n = 4 samples

Article Snippet: Specifically, the sections were treated with a mouse anti-β3-tubulin antibody (1:100, sc80016, Santa Cruz Biotechnology, USA) in combination with one of the following antibodies: rabbit anti-p-ErbB4 antibody (1:200, bs-3220R, Bioss, Beijing, China), and rabbit anti-synaptophysin (SYP) antibody (1:200, AF8091, Beyotime, Shanghai, China).

Techniques: Immunofluorescence, Western Blot, Derivative Assay, Comparison

ErbB4 small molecule agonist can improve hippocampal neuroinflammation in mice exposed to PS-MPs via the TLR4/NLRP3 pathway. ( A ) Levels of IBA1 were detected through immunofluorescence staining. ( B ) Levels of GFAP were detected through immunofluorescence staining. ( C ) Western blot analysis was utilized to detect protein levels associated with the TLR4/NLRP3 signaling pathway in the hippocampus of mice. ( D ) Statistical chart was generated to display the protein levels of TLR4/NLRP3. GFAP and IBA1 are both indicated in red, with a scale bar of 20 μm. Statistical analysis was conducted using one-way ANOVA followed by Tukey’s post hoc test for multiple comparisons, and the data are reported as means ± SEM, with significance levels denoted as * p < 0.05, ** p < 0.01, and *** p < 0.001. Each group comprised n = 4 samples

Journal: Journal of Neuroinflammation

Article Title: Targeted activation of ErbB4 receptor ameliorates neuronal deficits and neuroinflammation in a food-borne polystyrene microplastic exposed mouse model

doi: 10.1186/s12974-025-03406-6

Figure Lengend Snippet: ErbB4 small molecule agonist can improve hippocampal neuroinflammation in mice exposed to PS-MPs via the TLR4/NLRP3 pathway. ( A ) Levels of IBA1 were detected through immunofluorescence staining. ( B ) Levels of GFAP were detected through immunofluorescence staining. ( C ) Western blot analysis was utilized to detect protein levels associated with the TLR4/NLRP3 signaling pathway in the hippocampus of mice. ( D ) Statistical chart was generated to display the protein levels of TLR4/NLRP3. GFAP and IBA1 are both indicated in red, with a scale bar of 20 μm. Statistical analysis was conducted using one-way ANOVA followed by Tukey’s post hoc test for multiple comparisons, and the data are reported as means ± SEM, with significance levels denoted as * p < 0.05, ** p < 0.01, and *** p < 0.001. Each group comprised n = 4 samples

Article Snippet: Specifically, the sections were treated with a mouse anti-β3-tubulin antibody (1:100, sc80016, Santa Cruz Biotechnology, USA) in combination with one of the following antibodies: rabbit anti-p-ErbB4 antibody (1:200, bs-3220R, Bioss, Beijing, China), and rabbit anti-synaptophysin (SYP) antibody (1:200, AF8091, Beyotime, Shanghai, China).

Techniques: Immunofluorescence, Staining, Western Blot, Generated

The ErbB4 small molecule agonist ameliorates hippocampal neuron damage under pathological conditions induced by PS-MPs in vitro via the ErbB4 signaling pathway, and concurrently attenuates microglial activation through the TLR4/NLRP3 signaling pathway. ( A - D ) Following exposure to PS-MPs at a concentration of 100 µg/mL for 24 h, hippocampal neurons were subsequently treated with C11H7BrO3 at a concentration of 10 nM for an additional 24 h. ( A , C ) Protein expression levels associated with the ErbB4 signaling pathway, mitochondrial function, apoptosis, and synaptic integrity in hippocampal neurons were quantified using Western blot analysis. ( B , D ) Statistical representations of these protein expression levels were depicted in graphical form. ( E ) Oxidative stress markers in hippocampal neurons, including total superoxide dismutase (T-SOD), glutathione (GSH), glutathione peroxidase (GSH-Px), and malondialdehyde (MDA) levels, were evaluated. ( F ) Intracellular ATP levels in hippocampal neurons were also measured. ( G - H ) Microglial cells were co-cultured with supernatants derived from treated hippocampal neurons for 24 h. ( G ) Protein expression levels related to the TLR4/NLRP3 signaling pathway in microglial cells were assessed via Western blot analysis. ( H ) Statistical representations of these protein expression levels were also depicted in graphical form. Statistical analysis was conducted using one-way ANOVA followed by Tukey’s post hoc test for multiple comparisons, and data are presented as means ± SEM. Significance levels were denoted as * p < 0.05, ** p < 0.01, *** p < 0.001. A minimum sample size of n = 4–6 per group was utilized

Journal: Journal of Neuroinflammation

Article Title: Targeted activation of ErbB4 receptor ameliorates neuronal deficits and neuroinflammation in a food-borne polystyrene microplastic exposed mouse model

doi: 10.1186/s12974-025-03406-6

Figure Lengend Snippet: The ErbB4 small molecule agonist ameliorates hippocampal neuron damage under pathological conditions induced by PS-MPs in vitro via the ErbB4 signaling pathway, and concurrently attenuates microglial activation through the TLR4/NLRP3 signaling pathway. ( A - D ) Following exposure to PS-MPs at a concentration of 100 µg/mL for 24 h, hippocampal neurons were subsequently treated with C11H7BrO3 at a concentration of 10 nM for an additional 24 h. ( A , C ) Protein expression levels associated with the ErbB4 signaling pathway, mitochondrial function, apoptosis, and synaptic integrity in hippocampal neurons were quantified using Western blot analysis. ( B , D ) Statistical representations of these protein expression levels were depicted in graphical form. ( E ) Oxidative stress markers in hippocampal neurons, including total superoxide dismutase (T-SOD), glutathione (GSH), glutathione peroxidase (GSH-Px), and malondialdehyde (MDA) levels, were evaluated. ( F ) Intracellular ATP levels in hippocampal neurons were also measured. ( G - H ) Microglial cells were co-cultured with supernatants derived from treated hippocampal neurons for 24 h. ( G ) Protein expression levels related to the TLR4/NLRP3 signaling pathway in microglial cells were assessed via Western blot analysis. ( H ) Statistical representations of these protein expression levels were also depicted in graphical form. Statistical analysis was conducted using one-way ANOVA followed by Tukey’s post hoc test for multiple comparisons, and data are presented as means ± SEM. Significance levels were denoted as * p < 0.05, ** p < 0.01, *** p < 0.001. A minimum sample size of n = 4–6 per group was utilized

Article Snippet: Specifically, the sections were treated with a mouse anti-β3-tubulin antibody (1:100, sc80016, Santa Cruz Biotechnology, USA) in combination with one of the following antibodies: rabbit anti-p-ErbB4 antibody (1:200, bs-3220R, Bioss, Beijing, China), and rabbit anti-synaptophysin (SYP) antibody (1:200, AF8091, Beyotime, Shanghai, China).

Techniques: In Vitro, Activation Assay, Concentration Assay, Expressing, Western Blot, Cell Culture, Derivative Assay

The schematic diagram illustrates the impact of targeted activation of ErbB4 receptor on hippocampal neuronal damage, neuroinflammation, and cognitive functions in mice exposed to PS-MPs. The small molecule ErbB4 receptor agonist (E4A) binds to the ErbB4 receptor, initiating its downstream signaling pathway. This activation leads to the upregulation of SIRT3 protein expression, which enhances mitochondrial redox homeostasis, increases ATP production, and ameliorates mitochondrial dysfunction. Additionally, there is an upregulation of synaptic-related proteins, which contributes to the repair of synaptic damage and enhancement of synaptic function. As hippocampal neuronal function improves, the activation of the TLR4 receptor by pro-inflammatory factors in microglia is reduced, resulting in diminished phosphorylation of NF-κB and decreased activation of the NLRP3 inflammasome towards Caspase-1. Consequently, there is a reduction in the conversion of the IL-1β precursor to its mature form, thereby alleviating hippocampal neuroinflammation and ultimately enhancing the learning and cognitive functions of PS-MPs-exposed mice. The diagram was created with MedPeer ( www.medpeer.cn )

Journal: Journal of Neuroinflammation

Article Title: Targeted activation of ErbB4 receptor ameliorates neuronal deficits and neuroinflammation in a food-borne polystyrene microplastic exposed mouse model

doi: 10.1186/s12974-025-03406-6

Figure Lengend Snippet: The schematic diagram illustrates the impact of targeted activation of ErbB4 receptor on hippocampal neuronal damage, neuroinflammation, and cognitive functions in mice exposed to PS-MPs. The small molecule ErbB4 receptor agonist (E4A) binds to the ErbB4 receptor, initiating its downstream signaling pathway. This activation leads to the upregulation of SIRT3 protein expression, which enhances mitochondrial redox homeostasis, increases ATP production, and ameliorates mitochondrial dysfunction. Additionally, there is an upregulation of synaptic-related proteins, which contributes to the repair of synaptic damage and enhancement of synaptic function. As hippocampal neuronal function improves, the activation of the TLR4 receptor by pro-inflammatory factors in microglia is reduced, resulting in diminished phosphorylation of NF-κB and decreased activation of the NLRP3 inflammasome towards Caspase-1. Consequently, there is a reduction in the conversion of the IL-1β precursor to its mature form, thereby alleviating hippocampal neuroinflammation and ultimately enhancing the learning and cognitive functions of PS-MPs-exposed mice. The diagram was created with MedPeer ( www.medpeer.cn )

Article Snippet: Specifically, the sections were treated with a mouse anti-β3-tubulin antibody (1:100, sc80016, Santa Cruz Biotechnology, USA) in combination with one of the following antibodies: rabbit anti-p-ErbB4 antibody (1:200, bs-3220R, Bioss, Beijing, China), and rabbit anti-synaptophysin (SYP) antibody (1:200, AF8091, Beyotime, Shanghai, China).

Techniques: Activation Assay, Expressing