The most popular versions of the tool 5.0 and 4.1.The actual developer of the program is Bio-Rad Laboratories.
Biorad Gel Image Software Software Is SuitableThis PC software is suitable for 32-bit versions of Windows XPVista7810.Biorad Gel Image Software Download Was CheckedThis download was checked by our built-in antivirus and was rated as virus free.
The current installation package available for download occupies 284.1 MB on disk. It runs on the following Bio-Rad imaging systems: - Gel Doc EZ imager and Gel Doc XR - ChemiDoc MP and ChemiDoc XRS - GS-900 calibrated densitometer. Do you need a nice image for publication If not and if you see everything you need to see why worring (Sorry, if I possibly play down your problem.) Yes, I do need a nice image for publication. New Forum Archives (2009-):: SDS-PAGE and Western Blotting. What you will see is that the samples are not causing the lane width problems. For instance, on the first image, it is not the sample 1881 that is the skinny lane, but it is in the second image. Furthermore, the first lane is skinny on the first image, but it is the second lane that is skinny on the second image. Did you do a protein estimation to make sure equal amounts of total protein was added 2. ![]() ![]() Yes. 1b. Yes. 2. Yes. V for 80 min 3.0 A -Cole Ziegler-. Gels are precast from Bio-Rad and are less than two weeks old. That would be interesting if salt content was the issue because this same exact protocol worked fine until yesterday and today. Not ruling out the possibility of salt being the issue, its just weird that it is coming up now. Cole Ziegler-. Usually it depended on my samples I loaded onto the gel especially when it was a whole extract (e.g. Do you need a nice image for publication If not and if you see everything you need to see why worring (Sorry, if I possibly play down your problem.) -Papaver-. Biorad Gel Image Software Code Analysis ShowsAlso, because of the lane differences, my memcode analysis shows that the lanes are not loaded with the same amount of protein (even though they are all loaded with 10 ul). The reason why it is not equal between all lanes is because of the width differences. In this case, you can still analyse this image even if it isnt publication perfect. The image software I use (Quantity ONE from BioRad) measures band intensity x volume (of the pixelated bands after chemiluminescent exposures. Therefore, if you had the same sample volume but different lanes (one wide, one narrow), you would expect to see the narrow one being more intense (protein jam-packed in that small area) vs.
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