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Key Product Details
Applications
Immunohistochemistry
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Product Specifications
Application Notes
Stable chromogen/substrate solution to be used in conjunction with peroxidase-based immunostaining systems. Specimens stained using AEC Chromogen/Substrate cannot be dehydrated in ethanol and hence need to be mounted in an aqueous based mounting medium.
Scientific Data Images for AEC Chromogen/Substrate
Immunohistochemistry-Paraffin: AEC Chromogen/Substrate [NB900-79773]
Immunohistochemistry-Paraffin: AEC Chromogen/Substrate [NB900-79773] - Formalin fixed paraffin embedded human tonsil stained with high molecular weight Cytokeratin ab labelled with AEC Chromogen/Substrate (NB900-79773)Formulation, Preparation, and Storage
Concentration
Please see the protocols for proper use of this product. If no protocol is available, contact technical services for assistance.
Shipping
The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Storage
Store at 4C. Do not freeze.
Background: AEC Chromogen/Substrate
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Product Documents for AEC Chromogen/Substrate
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for AEC Chromogen/Substrate
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Support products are guaranteed for 6 months from date of receipt.
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Protocols
View specific protocols for AEC Chromogen/Substrate (NB900-79773):
AEC Chromogen/Substrate Kit Protocol (NB900-79773):
Staining Procedure
1. Once sections have been incubated with peroxidase, wash sections with wash buffer.
2. Wipe slides to remove excess buffer. Add enough drops of AEC Chromogen/Substrate to cover tissue sections.
3. Incubate for 5-15 minutes at room temperature.
4. For best results, observe reaction under a microscope for signal development.
5. Once desired signal to noise ratio is achieved, stop reaction by washing slides in DI H2O.
Staining Procedure
1. Once sections have been incubated with peroxidase, wash sections with wash buffer.
2. Wipe slides to remove excess buffer. Add enough drops of AEC Chromogen/Substrate to cover tissue sections.
3. Incubate for 5-15 minutes at room temperature.
4. For best results, observe reaction under a microscope for signal development.
5. Once desired signal to noise ratio is achieved, stop reaction by washing slides in DI H2O.
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
- 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
FAQs
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