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Assay Development & Protocols
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Western Blot on a 500kDa Protein [View Printable]
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hulkster
Group: Member Posts: 2 Joined: Jul 15, 2008
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Hi everyone,
I am currently trying to resolve a 500kDa protein, but to no avail. I am using a 7.5% polyacrylamide gel in a 1X Tris glycine buffer.
Moreover, I can't seem to find a protein ladder suitable for a molecular weight of this size. NuPage makes one called the HiMark, but its for tris-acetate gels (ones only they supply)
Any suggestions??
Thanks
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| Posted Jul 15, 2008, 11:11 AM |
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samm
Group: Moderators Posts: 418 Joined: Mar 03, 2005
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Whoa! My largest has been ~400 (PC1) - best advice: 4% gel - handle it very gently for transfer, silanize (RainX works) plates, place membrane on gel (not the other way around), and wet transfer overnight - I'll check and let you know the voltages). Also - is this a native gel, or a denaturing/non-denaturing SDS?
For the marker, thyroglobulin may be a good choice. You may need to add that to a std commercial marker (max ~200-220 kDa). Antibodies to bovine thyroglobulin are also available if you want to use it as a protein loading ctrl.
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| Posted Jul 15, 2008, 22:04 PM |
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hulkster
Group: Member Posts: 2 Joined: Jul 15, 2008
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| samm said: | Whoa! My largest has been ~400 (PC1) - best advice: 4% gel - handle it very gently for transfer, silanize (RainX works) plates, place membrane on gel (not the other way around), and wet transfer overnight - I'll check and let you know the voltages). Also - is this a native gel, or a denaturing/non-denaturing SDS?
For the marker, thyroglobulin may be a good choice. You may need to add that to a std commercial marker (max ~200-220 kDa). Antibodies to bovine thyroglobulin are also available if you want to use it as a protein loading ctrl. |
I know, this thing is huge... It's a denaturing SDS.... Transferring overnight seems like a good idea, thanks for the input and I hope to hear what voltage you had it at! Also, how long /what voltage did you run the 4%? Also, what type of gel did you use? Thanks again
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| Posted Jul 15, 2008, 21:48 PM |
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samm
Group: Moderators Posts: 418 Joined: Mar 03, 2005
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For the overnight (~13-14 h) transfer, a) use chilled buffers, and do the transfer in a cold room b) for a mini-~8-12 cm gel (I'd used the BioRad miniProtean2 most often, but anything similar will do), 30 V transfer setting (constant voltage: usually ~90mA initial current). I'd used both denaturing and non-denaturing SDS PA gels - its different for native gels, which is why I asked. You might also try out something like Amresco's 5% self forming gradient NEXTGel (ISCBioexpress) - fairly cheap (~$26 for 10 gels rgts - all you need is APS and TEMED) - they are a little less fragile than the 4% gels, but still require VERY careful handling. All the best, and let us know when you manage to tame it - including any tweaks!
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| Posted Jul 19, 2008, 9:39 AM |
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