Embed stain in UOF

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Aug 6th, 2022
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Editing UOF is fast and straightforward using DocHub. Skip downloading software to your computer and make alterations with our drag and drop document editor in a few quick steps. DocHub is more than just a PDF editor. Users praise it for its convenience and powerful features that you can use on desktop and mobile devices. You can annotate documents, create fillable forms, use eSignatures, and email records for completion to other people. All of this, combined with a competitive cost, makes DocHub the perfect decision to embed stain in UOF files effortlessly.

Your quick guide to embed stain in UOF with DocHub:

  1. Add your UOF file into your DocHub profile.
  2. After you select your file, click it to open it in our editor.
  3. Use intuitive editing tools to make any alterations to your record.
  4. Once completed, click Download/Export and save your UOF to your device or cloud storage.
  5. Store your files in your Documents folder for easy access from any device.

Make your next tasks even easier by converting your documents into reusable web templates. Don't worry about the security of your records, as we securely keep them in the DocHub cloud.

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How to embed stain in UOF

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The overall goal of this video is to demonstrate an immunohistochemistry protocol for paraffin-embedded tissue sections. This is accomplished by first slicing paraffin infiltrated tissue on a microtome and then mounting the sections onto charged slides. The sections are then deparaffinized and rehydrated before performing antigen unmasking to remove the cross-links formed by fixation. Next, a specific antibody is applied to the sections to bind to its target epitope prior to chromogenic staining. After dehydrating the sections, the final step is to mount the sections for microscopic analysis. Ultimately, antibodies are used to detect and analyze protein expression while maintaining the composition, cellular characteristics, and structure of native tissue. Generally, individuals new to this method will struggle because there are so many steps in the procedure and variations in each step can have an impact on staining. (CST) antibodies that are validated for immunohistochemistry are deve

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Martius Scarlet Blue (MSB) staining technique is used for fibrin visualization, especially of older clusters. This method is a modified Masson Trichrome method and it is ideal for studying docHub tissue and vascular pathology.
Massons Trichrome Staining is a histological staining method used for selectively stain collagen, collagen fibers, fibrin, muscles, and erythrocytes. It uses three stains for staining hence the term Trichrome. These are Weigerts Hematoxylin, Biebrich scarlet-acid fuschin solution, and Aniline blue.
3.3 Tissue Orientation and Embedding The correct orientation of the tissue is very important for proper cutting and microscopic examination. Tissue is usually placed as flat on the central part of the mould. It should be oriented in such a way so that cutting is easy by the knife of the microtome.
Movats Pentachrome is a complex stain that highlights fibrin, mucin, and collagen in a tissue section. The cellular structures on a slide will be stained as follows: nuclei and elastic fibers black, fibrin intense red, muscle red, collagen and reticular fibers yellow, and ground substance mucin blue.
Place in crystal scarlet for 10 minutes. Differentiate with phosphotungstic acid until only fibrin is red (up to 10 minutes). Place in methyl blue until collagen is blue (up to 10 minutes). Rinse briefly with 1% aqueous acetic acid.
Special Stains Massons Trichrome. The trichrome stain helps to highlight the supporting collagenous stroma in sections from a variety of organs. Verhoffs Elastic Stain. Reticulin Stain. Giemsa Stain.
Collagen staining by Picrosirius red dye in various mouse reproductive tissues and fetal membrane. Red to pink is collagen stain. Yellow is cytoplasm.
Fibrin is an acidophil material, that is, it is stained by acid dyes and is pink in an H E. From the histological perspective, blood clots are pretty obvious in most cases, and the fibrin can often be seen in an H E as distinctly pink but less brilliant than the erythrocytes.

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