Features
Essential features
- Exceptional quality, comprehensive range, and rigorous validation processes distinguish our staining kits and secondary antibodies.
- Stringent quality control measures guarantee minimal background staining and robust signal amplification.
- Provides researchers with the clarity and precision needed for reliable results.
- Our kits come with all the necessary reagents and detailed protocols for easy, reliable, and reproducible results.
- Our double- and triple-staining kits conserve valuable samples and streamline workflows, significantly reducing the time and effort needed for multiple separate staining procedures whilst offering a more comprehensive understanding of cellular interactions and tissue architecture.
Applications
Applications
- Neuroscience: Facilitates the study of co-localization of neuronal markers, aiding in the exploration of neural networks and pathways.
- Oncology: Enhances the understanding of intricate cellular interactions and tumor microenvironments.
- Pathological studies: Provides detailed insights into tissue architecture, assisting in the analysis of various diseases.
- Complex tissue analysis: Streamlines the process of detecting multiple antigens within a single tissue section, saving time and resources.
- Cellular interactions: Offers a comprehensive understanding of cellular interactions, which is critical for advancing various research fields.
What is an IHC kit?
An IHC kit includes a set of reagents and tools specifically designed to detect antigens in tissue sections by immunohistochemistry. These kits typically contain the conjugated secondary antibody, buffers, and detection substrates.
What types of samples can be used for IHC?
IHC can be performed on various types of samples, such as paraffin-embedded tissue, frozen tissue sections, and cytology specimens. Each sample type requires specific preparation and handling techniques for optimal results.
What is the difference between IHC and immunofluorescence (IF)?
IHC utilizes chromogenic detection methods with colored enzyme substrates to visualize antigens, while IF uses fluorescent dyes. The choice between the two depends on the desired visualization method and sensitivity requirements.
Can IHC be used to detect multiple markers in the same tissue?
Yes, IHC can be employed to detect multiple markers within a single tissue section using techniques like double or triple staining. This allows for the simultaneous visualization of different antigens in the same sample.
What is the purpose of blocking in IHC?
Blocking in IHC is used to prevent the non-specific binding of antibodies to tissues, reducing background staining and enhancing the specificity of the signal. This step is crucial for achieving accurate and clear staining results.
Which reagent is commonly used in immunohistochemistry?
Primary and secondary antibodies are commonly used for detection in immunohistochemistry, along with buffers and substrates. These reagents work together to visualize the targeted antigens in tissue sections. Examples of substrates used in chromogenic detection include 3,3’-diaminobenzidine (DAB, brown), 3-amino-9-ethyl carbazole (AEC, red), tetramethylbenzidine (TMB, blue), 5-bromo-4-chloro-3-indolyl phosphate/nitro blue tetrazolium (BCIP/NBT, blue), and StayGreen (green), among others, each producing distinct colors depending on the enzyme used.
What markers are used in IHC?
Markers used in IHC include a wide range of proteins, peptides, and other antigens that are relevant to the specific research focus. These markers help identify and study various biological processes and disease states.
Can IHC be used for quantitative analysis?
Yes, IHC can be utilized for quantitative analysis by measuring the intensity and distribution of staining to assess antigen expression levels. This approach allows researchers to quantify and compare antigen presence in different samples.