Documents

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    Whitepaper: An end-to-end workflow for exploring spatial biology through multiplex IHC
    Whitepaper
    Multiplex immunohistochemistry (IHC) technologies are powerful tools to visualize multiple markers in the same tissue sample. These techniques, which include tyramide signal amplification and cyclic immunofluorescence, help scientists understand the cells that make up a tissue, what markers they express, their spatial distribution, and their potential interactions with one another. These methods depend on antibodies that are specific to the target, produce a clean signal, and have low background.
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    Cell Lysate Protocols eBook
    Ebook
    This eBook is a comprehensive resource for cell lysate preparation. It covers cell lysis using RIPA and NETN, as well as specific protocols for nuclear extract preparation and immunoprecipitation.
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    Drugs of Abuse Pairing Guide
    Ebook
    At Fortis Life Sciences®, we understand the importance of accurate and reliable rapid diagnostic tests for detecting drugs of abuse. That's why we are a global supplier of matched pairs of drug test reagents for use in lateral flow formats. Accelerate your development timeline by referencing this pairing guide for the selection of compatible drug test reagents.
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    VHH Antibodies: Novel Engineering Strategies Beget Diverse Applications
    Whitepaper
    Single-domain antibodies, also known as VHH, are a monomeric variable antibody domain. In research, therapeutic, and diagnostic applications, these single-domain antibodies have advantages over conventional antibodies. Applications of VHH include multiplex imaging, as a component of cell therapies or as a therapeutic modality themselves, and immunoassays for diagnostic and environmental monitoring assays.
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    Ensuring Antibody Specificity and Reproducibility: The Six Pillars of Antibody Validation
    Whitepaper
    An antibody is only useful if you can trust the data it generates. How do you know that your antibody is truly binding your protein of interest? What if the antibody cross-reacts with non-target proteins? Or if the antibody generates an unexpected banding pattern?