Neurogranin Antibody (898502)
R&D Systems | Catalog # MAB7947
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Key Product Details
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Met1-Asp78
Accession # Q92686
Specificity
Clonality
Host
Isotype
Scientific Data Images for Neurogranin Antibody (898502)
Detection of Human, Mouse, and Rat Neurogranin by Western Blot.
Western blot shows lysates of human brain (motor cortex), mouse brain, and rat brain. PVDF membrane was probed with 2 µg/mL of Mouse Anti-Human/Mouse/Rat Neurogranin Monoclonal Antibody (Catalog # MAB7947) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (HAF018). A specific band was detected for Neurogranin at approximately 13-14 kDa (as indicated). This experiment was conducted under reducing conditions and using Western Blot Buffer Group 1.Neurogranin in Human Cortex.
Neurogranin was detected in formalin fixed paraffin-embedded sections of human cortex using Mouse Anti-Human/Mouse/Rat Neurogranin Monoclonal Antibody (Catalog # MAB7947) at 15 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Mouse HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS002) and counterstained with hematoxylin (blue). Specific staining was localized to neuronal cell bodies and dendrites. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.Neurogranin in Mouse Brain.
Neurogranin was detected in perfusion fixed frozen sections of mouse brain using Mouse Anti-Human/Mouse/Rat Neurogranin Monoclonal Antibody (Catalog # MAB7947) at 25 µg/mL overnight at 4 °C. Tissue was stained using the NorthernLights™ 557-conjugated Anti-Mouse IgG Secondary Antibody (red; Catalog # NL007) and counterstained with DAPI (blue). Specific staining was localized to cytoplasm in neurons. View our protocol for Fluorescent IHC Staining of Frozen Tissue Sections.Neurogranin in Rat Brain.
Neurogranin was detected in perfusion fixed frozen sections of rat brain using Mouse Anti-Human/Mouse/Rat Neurogranin Monoclonal Antibody (Catalog # MAB7947) at 25 µg/mL overnight at 4 °C. Tissue was stained using the NorthernLights™ 557-conjugated Anti-Mouse IgG Secondary Antibody (red; Catalog # NL007) and counterstained with DAPI (blue). Specific staining was localized to cytoplasm in neurons. View our protocol for Fluorescent IHC Staining of Frozen Tissue Sections.Detection of Neurogranin by Immunohistochemistry
Expression pattern of Nrg1 in the cerebral cortex. A The densities of Nrg1-positive cells in different regions of cerebral cortex from 2-month-old Nrg1-reporting mice. P < 0.0001, n = 3 mice (6 slices) for Au and LE, n = 3 mice (9 slices) for other cortical regions, one-way-ANOVA. B The percentage of Nrg1-positive cells in different layers among total Nrg1-positive cells from multiple cortical regions. Layer factor P < 0.0001, region factor P > 0.99, n = 3 mice (9 slices) for each cortical region, two-way-ANOVA. C Diagram of mouse brain sagittal section (top) and coronal section (bottom). The line in the sagittal section diagram indicates the position of the coronal section. The rectangle indicates the brain region shown in panel D. D Fluorescent images of tdTomato in the SS1. Scale bar, 300 μm. E Fluorescent images of tdTomato, NRGN and NeuN, from the rectangle in panel D. Scale bar, 150 μm. F Fluorescent images of tdTomato, NRGN and NeuN, enlarged from the rectangle in panel E. Arrows indicate Nrg1-positive pyramidal neurons. Scale bar, 50 μm. G Fluorescent images of tdTomato and gad67-GFP in the SS1. Scale bar, 50 μm. Au: auditory cortex; RS: retrosplenial cortex; Cg1: cingulate cortex, area 1; Pir: piriform cortex; SS1: primary somatosensory cortex; LE: lateral entorhinal cortex; SS2: secondary somatosensory cortex; M1: primary motor cortex; M2: secondary motor cortex; PtA: parietal association cortex Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/37147705), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Neurogranin Antibody (898502)
Immunohistochemistry
Sample: Immersion fixed paraffin-embedded sections of human cortex, and perfusion fixed frozen sections of mouse brain and rat brain
Western Blot
Sample: Human brain (motor cortex), mouse brain, and rat brain
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.5 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: Neurogranin
Alternate Names
Gene Symbol
UniProt
Additional Neurogranin Products
Product Documents for Neurogranin Antibody (898502)
Certificate of Analysis
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Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Neurogranin Antibody (898502)
For research use only
Citations for Neurogranin Antibody (898502)
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars