B-Raf Antibody (IHC600) - V600-E Mutation
Novus Biologicals | Catalog # NBP3-00517
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Species Reactivity
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Immunogen
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Scientific Data Images for B-Raf Antibody (IHC600) - V600-E Mutation
Immunohistochemistry-Paraffin: B-Raf Antibody (IHC600) - V600-E Mutation [NBP3-00517]
Immunohistochemistry-Paraffin: B-Raf Antibody (IHC600) - V600-E Mutation [NBP3-00517] - Staining of B-Raf Antibody (IHC600) in thyroid papillary carcinoma with BRAF V600-E mutationApplications for B-Raf Antibody (IHC600) - V600-E Mutation
Immunohistochemistry
Immunohistochemistry-Paraffin
Formulation, Preparation, and Storage
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Background: B-Raf
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Additional B-Raf Products
Product Documents for B-Raf Antibody (IHC600) - V600-E Mutation
Certificate of Analysis
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Product Specific Notices for B-Raf Antibody (IHC600) - V600-E Mutation
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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Protocols
View specific protocols for B-Raf Antibody (IHC600) - V600-E Mutation (NBP3-00517):
Immunohistochemistry Protocol
Specimen Collection and Preparation for Analysis
Each tissue section should be fixed with 10% neutral buffered formalin, cut to the applicable thickness (4um), and placed on a glass slide that is positively charged. The prepared slide may then be baked for a minimum of 30 minutes in a 53-65 degrees C oven (do not exceed 24 hours).
Recommended Staining Protocols
Manual Use:
1. Blocking: If HRP is used, block with peroxidase blocking solution for 10 to 15 minutes at room temperature. Use alkaline phosphatase blocking solution if using an AP system.
2. Primary Antibody: Apply antibody directly (Predilute) or dilute antibody at 1:30 (Concentrate) before applying. Incubate antibody for 30 to 60 minutes at room temperature or overnight at 4C.
3. Secondary Antibody: Incubate for 20 to 30 minutes at room temperature.
4. Substrate Development: Incubate DAB or Fast Red for 5 to 10 minutes at room temperature.
5. Counterstain: Counterstain with hematoxylin for 0.5 to 5 minutes, depending on the hematoxylin used. Rinse with distilled water and bluing solution for 30 seconds.
6. Dehydrate and apply coverslip.
For all automated IHC staining systems, refer to the corresponding user manual for specific instructions.
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
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- View all Protocols, Troubleshooting, Illustrated assays and Webinars