Blot data in 602

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Aug 6th, 2022
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How to blot data in 602

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hello everyone in this video today iamp;#39;m going to talk to you about how to perform the quantification of western blots using image software okay so first to upload the image into the images software you will either go to file open and then you open your image or you can simply drag your image uh to to to the software like the way i did okay so then after you did this do this then if you see something like this with your your your bands in your version of launch operating white then what you will do is you will simply go to edit and you will go to invert okay so then now you have the bands like this the problem with this is that this if you look at this block here these bands they donamp;#39;t appear in a straight line right so they are like a little bit tilted so what you will do then then you will go to image and then you will go to a transform and then you will go to rotate and then you have to decide at what degree you should rotate your image for now iamp;#39;m just going t

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To know how to analyze western blot data, Look for the sizes of the bands. These will be represented by a number, either followed by kDa or preceded by p. This is the size of the protein which has been detected and is the scale on which the proteins are separated in a Western blot.
The currently licensed Du Pont Western blot test specifies that the test result should be interpreted as positive only when the detected bands include p24 and p31, and gp41 or gp120/160 (12) (see Table 2).
A western blot is a laboratory method used to detect specific protein molecules from among a mixture of proteins. This mixture can include all of the proteins associated with a particular tissue or cell type.
Quantitating a western blot refers to the measurement of the signal emitted by your protein band(s) of interest. The signal intensity of the band is directly proportional to the concentration of your target protein.
To this end, once a western blot has been imaged, it can then be analyzed. To do this, researchers use a technique called densitometry to measure the relative amount of a specific protein for a given experimental sample on the blot by comparing it with a control or another protein.

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