cortical regions Search Results


cortical regions  (The Virtual Brain)
90
The Virtual Brain cortical regions
Cortical Regions, supplied by The Virtual Brain, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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time-intensity curve (tic) of renal cortical regions of interest (roi)  (TOMTEC IMAGING SYSTEMS GMBH)
90
TOMTEC IMAGING SYSTEMS GMBH time-intensity curve (tic) of renal cortical regions of interest (roi)
Time Intensity Curve (Tic) Of Renal Cortical Regions Of Interest (Roi), supplied by TOMTEC IMAGING SYSTEMS GMBH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cryopreserved rat hippocampal/cortical regions  (BrainBits LLC)
90
BrainBits LLC cryopreserved rat hippocampal/cortical regions
Navβ2 is required for BACE1 activity-dependent regulation of Nav1.1 levels. <t>Primary</t> <t>neuronal</t> <t>culture</t> (14 days in vitro) from Navβ2-null mice (Navβ2 KO), wild-type control mice (WT), and wild-type <t>rat</t> were treated with control vehicle (DMSO) or BACE inhibitors (DR9 and/or inhibitor IV) for 48–72 h. Nav1.1 protein levels were analyzed by Western blot. A, upper panel, Nav1.1 Western blot analysis of rat primary neurons (14 days in vitro) treated with various concentrations of DR9 and control vehicle DMSO for 72 h; lower panel, quantitative analysis of Nav1.1 protein levels. B, representative Western blot showing changes in Nav1.1 levels upon BACE1 inhibitor treatment in cultured WT neurons. C, quantitative analysis of Nav1.1 protein levels upon BACE1 inhibitor treatment in cultured WT neurons. D, representative Western blot showing Nav1.1 levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. E, quantitative analysis of Nav1.1 protein levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. One-way ANOVA followed by a post hoc Tukey's test was used for statistical analysis (*, p < 0.05; n = 3 per each condition).
Cryopreserved Rat Hippocampal/Cortical Regions, supplied by BrainBits LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cortical+regions/cryopreserved+rat+hippocampal+cortical+regions/pmc03048697-73-1-12
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cortical and subcortical regions comprising the face-processing network  (Scherf GmbH)
90
Scherf GmbH cortical and subcortical regions comprising the face-processing network
Navβ2 is required for BACE1 activity-dependent regulation of Nav1.1 levels. <t>Primary</t> <t>neuronal</t> <t>culture</t> (14 days in vitro) from Navβ2-null mice (Navβ2 KO), wild-type control mice (WT), and wild-type <t>rat</t> were treated with control vehicle (DMSO) or BACE inhibitors (DR9 and/or inhibitor IV) for 48–72 h. Nav1.1 protein levels were analyzed by Western blot. A, upper panel, Nav1.1 Western blot analysis of rat primary neurons (14 days in vitro) treated with various concentrations of DR9 and control vehicle DMSO for 72 h; lower panel, quantitative analysis of Nav1.1 protein levels. B, representative Western blot showing changes in Nav1.1 levels upon BACE1 inhibitor treatment in cultured WT neurons. C, quantitative analysis of Nav1.1 protein levels upon BACE1 inhibitor treatment in cultured WT neurons. D, representative Western blot showing Nav1.1 levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. E, quantitative analysis of Nav1.1 protein levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. One-way ANOVA followed by a post hoc Tukey's test was used for statistical analysis (*, p < 0.05; n = 3 per each condition).
Cortical And Subcortical Regions Comprising The Face Processing Network, supplied by Scherf GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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prefrontal cortical regions  (Thomann GmbH)
90
Thomann GmbH prefrontal cortical regions
Navβ2 is required for BACE1 activity-dependent regulation of Nav1.1 levels. <t>Primary</t> <t>neuronal</t> <t>culture</t> (14 days in vitro) from Navβ2-null mice (Navβ2 KO), wild-type control mice (WT), and wild-type <t>rat</t> were treated with control vehicle (DMSO) or BACE inhibitors (DR9 and/or inhibitor IV) for 48–72 h. Nav1.1 protein levels were analyzed by Western blot. A, upper panel, Nav1.1 Western blot analysis of rat primary neurons (14 days in vitro) treated with various concentrations of DR9 and control vehicle DMSO for 72 h; lower panel, quantitative analysis of Nav1.1 protein levels. B, representative Western blot showing changes in Nav1.1 levels upon BACE1 inhibitor treatment in cultured WT neurons. C, quantitative analysis of Nav1.1 protein levels upon BACE1 inhibitor treatment in cultured WT neurons. D, representative Western blot showing Nav1.1 levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. E, quantitative analysis of Nav1.1 protein levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. One-way ANOVA followed by a post hoc Tukey's test was used for statistical analysis (*, p < 0.05; n = 3 per each condition).
Prefrontal Cortical Regions, supplied by Thomann GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cortical+regions/prefrontal+cortical+regions/pm30248379-31-30-37
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parcellated cortical regions  (Johns Hopkins HealthCare)
90
Johns Hopkins HealthCare parcellated cortical regions
Navβ2 is required for BACE1 activity-dependent regulation of Nav1.1 levels. <t>Primary</t> <t>neuronal</t> <t>culture</t> (14 days in vitro) from Navβ2-null mice (Navβ2 KO), wild-type control mice (WT), and wild-type <t>rat</t> were treated with control vehicle (DMSO) or BACE inhibitors (DR9 and/or inhibitor IV) for 48–72 h. Nav1.1 protein levels were analyzed by Western blot. A, upper panel, Nav1.1 Western blot analysis of rat primary neurons (14 days in vitro) treated with various concentrations of DR9 and control vehicle DMSO for 72 h; lower panel, quantitative analysis of Nav1.1 protein levels. B, representative Western blot showing changes in Nav1.1 levels upon BACE1 inhibitor treatment in cultured WT neurons. C, quantitative analysis of Nav1.1 protein levels upon BACE1 inhibitor treatment in cultured WT neurons. D, representative Western blot showing Nav1.1 levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. E, quantitative analysis of Nav1.1 protein levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. One-way ANOVA followed by a post hoc Tukey's test was used for statistical analysis (*, p < 0.05; n = 3 per each condition).
Parcellated Cortical Regions, supplied by Johns Hopkins HealthCare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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novel genes differentially expressed in cortical regions during late neurogenesis  (CHOWDHURY AND CO LUTON LIMITED)
90
CHOWDHURY AND CO LUTON LIMITED novel genes differentially expressed in cortical regions during late neurogenesis
Navβ2 is required for BACE1 activity-dependent regulation of Nav1.1 levels. <t>Primary</t> <t>neuronal</t> <t>culture</t> (14 days in vitro) from Navβ2-null mice (Navβ2 KO), wild-type control mice (WT), and wild-type <t>rat</t> were treated with control vehicle (DMSO) or BACE inhibitors (DR9 and/or inhibitor IV) for 48–72 h. Nav1.1 protein levels were analyzed by Western blot. A, upper panel, Nav1.1 Western blot analysis of rat primary neurons (14 days in vitro) treated with various concentrations of DR9 and control vehicle DMSO for 72 h; lower panel, quantitative analysis of Nav1.1 protein levels. B, representative Western blot showing changes in Nav1.1 levels upon BACE1 inhibitor treatment in cultured WT neurons. C, quantitative analysis of Nav1.1 protein levels upon BACE1 inhibitor treatment in cultured WT neurons. D, representative Western blot showing Nav1.1 levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. E, quantitative analysis of Nav1.1 protein levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. One-way ANOVA followed by a post hoc Tukey's test was used for statistical analysis (*, p < 0.05; n = 3 per each condition).
Novel Genes Differentially Expressed In Cortical Regions During Late Neurogenesis, supplied by CHOWDHURY AND CO LUTON LIMITED, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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particular cortical regions  (METTLER TOLEDO)
90
METTLER TOLEDO particular cortical regions
Navβ2 is required for BACE1 activity-dependent regulation of Nav1.1 levels. <t>Primary</t> <t>neuronal</t> <t>culture</t> (14 days in vitro) from Navβ2-null mice (Navβ2 KO), wild-type control mice (WT), and wild-type <t>rat</t> were treated with control vehicle (DMSO) or BACE inhibitors (DR9 and/or inhibitor IV) for 48–72 h. Nav1.1 protein levels were analyzed by Western blot. A, upper panel, Nav1.1 Western blot analysis of rat primary neurons (14 days in vitro) treated with various concentrations of DR9 and control vehicle DMSO for 72 h; lower panel, quantitative analysis of Nav1.1 protein levels. B, representative Western blot showing changes in Nav1.1 levels upon BACE1 inhibitor treatment in cultured WT neurons. C, quantitative analysis of Nav1.1 protein levels upon BACE1 inhibitor treatment in cultured WT neurons. D, representative Western blot showing Nav1.1 levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. E, quantitative analysis of Nav1.1 protein levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. One-way ANOVA followed by a post hoc Tukey's test was used for statistical analysis (*, p < 0.05; n = 3 per each condition).
Particular Cortical Regions, supplied by METTLER TOLEDO, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Navβ2 is required for BACE1 activity-dependent regulation of Nav1.1 levels. Primary neuronal culture (14 days in vitro) from Navβ2-null mice (Navβ2 KO), wild-type control mice (WT), and wild-type rat were treated with control vehicle (DMSO) or BACE inhibitors (DR9 and/or inhibitor IV) for 48–72 h. Nav1.1 protein levels were analyzed by Western blot. A, upper panel, Nav1.1 Western blot analysis of rat primary neurons (14 days in vitro) treated with various concentrations of DR9 and control vehicle DMSO for 72 h; lower panel, quantitative analysis of Nav1.1 protein levels. B, representative Western blot showing changes in Nav1.1 levels upon BACE1 inhibitor treatment in cultured WT neurons. C, quantitative analysis of Nav1.1 protein levels upon BACE1 inhibitor treatment in cultured WT neurons. D, representative Western blot showing Nav1.1 levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. E, quantitative analysis of Nav1.1 protein levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. One-way ANOVA followed by a post hoc Tukey's test was used for statistical analysis (*, p < 0.05; n = 3 per each condition).

Journal: The Journal of Biological Chemistry

Article Title: Reduced Sodium Channel Na v 1.1 Levels in BACE1-null Mice *

doi: 10.1074/jbc.M110.134692

Figure Lengend Snippet: Navβ2 is required for BACE1 activity-dependent regulation of Nav1.1 levels. Primary neuronal culture (14 days in vitro) from Navβ2-null mice (Navβ2 KO), wild-type control mice (WT), and wild-type rat were treated with control vehicle (DMSO) or BACE inhibitors (DR9 and/or inhibitor IV) for 48–72 h. Nav1.1 protein levels were analyzed by Western blot. A, upper panel, Nav1.1 Western blot analysis of rat primary neurons (14 days in vitro) treated with various concentrations of DR9 and control vehicle DMSO for 72 h; lower panel, quantitative analysis of Nav1.1 protein levels. B, representative Western blot showing changes in Nav1.1 levels upon BACE1 inhibitor treatment in cultured WT neurons. C, quantitative analysis of Nav1.1 protein levels upon BACE1 inhibitor treatment in cultured WT neurons. D, representative Western blot showing Nav1.1 levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. E, quantitative analysis of Nav1.1 protein levels of cultured Navβ2 KO neurons treated with DMSO, DR9, or inhibitor IV. One-way ANOVA followed by a post hoc Tukey's test was used for statistical analysis (*, p < 0.05; n = 3 per each condition).

Article Snippet: For rat primary neuronal culture, cryopreserved rat hippocampal/cortical regions were purchased from BrainBits (Springfield, IL), dissociated, and plated on poly- d -lysine/laminin-coated plates.

Techniques: Activity Assay, In Vitro, Control, Western Blot, Cell Culture