Blot size in ASC in a few clicks

Aug 6th, 2022
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01. Upload a document from your computer or cloud storage.
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02. Add text, images, drawings, shapes, and more.
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03. Sign your document online in a few clicks.
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04. Send, export, fax, download, or print out your document.

Blot size in ASC efficiently and securely

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DocHub makes it quick and simple to blot size in ASC. No need to download any software – simply add your ASC to your profile, use the simple drag-and-drop editor, and quickly make edits. You can even work on your desktop or mobile device to adjust your document online from anywhere. That's not all; DocHub is more than just an editor. It's an all-in-one document management solution with form creating, eSignature features, and the option to enable others fill in and eSign documents.

How to blot size in ASC using DocHub:

  1. Upload your ASC to your profile by clicking the New Document and selecting how you want to add your ASC file.
  2. Open your file in our editor.
  3. Make your desired adjustments using drag and drop tools.
  4. Once completed, click Download/Export and save your ASC to your device or cloud storage.
  5. Share your record with others using email or an active link.

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How to blot size in ASC

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Western blots can also be used to evaluate the size of a protein of interest, and to measure the amount of protein expression. This procedure was named for its similarity to the previously invented method known as the Southern blot.
ASC/TMS1 is synthesized as a 195-amino acid (aa) protein with a theoretical weight of 22 kDa. Structurally the protein contains a N-terminal PYD (pyrin domain) and C-terminal CARD (caspase-recruitment domain) (1-4).
Most laboratories use a range of 2040g of total protein for loading homogenates for western blotting.
Determine how much protein to load (Recommended: 10-50 g/lane) and add an equal volume 2X Laemmli buffer. Reduce and denature the samples by boiling the lysates in Laemmli Buffer at 95-100˚C for 5 minutes.
To obtain linear signals with the majority of western blots, we recommend loading smaller amounts of protein sample between 1 and 10 g per well. To avoid under- or overloading samples, determine the protein concentration of each sample prior to electrophoresis with a compatible protein assay.
A typical Western blot, or immunoblot, relies upon a purified, semi-purified, or crude extract of cellular proteins containing a target protein that can be detected by antibodies. Several key steps are required to take the sample from the cellular starting point to a detectible band on a Western blot.
ASC specks can be observed as they docHub a size of around 1 m and in most cells only one speck forms upon inflammasome activation. Hence, ASC speck formation can be used as a simple upstream readout for inflammasome activation.
it depends on the cell concentration of the proteins that you are looking for. As example for ubiquitous protein like actin or tubulin also 10*10e4 is well enought to run multiple WB. For less expressed protein, 1*10e6 should fit well.

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