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Top : New Forum Archives (2009-): : Electrophoresis
1. Problems for DNA agarose gel visualization with a gel documentation system - (reply: 9)
2. Weird agarose melting at standard conditions - just at the wells?? - (reply: 1)
3. Faint band and primer dimer in PCR - (reply: 1)
4. Dye does not separe in acrylamide gel - (reply: 2)
5. 5X, 6X sds gel loading buffer - (reply: 4)
6. ethidium bromide contact - (reply: 1)
7. lower part of the gel was not stained - (reply: 7)
8. bands becoming wavy with colour of the dye changing to yellow - (reply: 1)
9. Fragment sizes smaller than expected - (reply: 1)
10. Electrophoresis problem: Frowning bands and smeary ladder - (reply: 1)
11. Agarose Gel consistency issues - (reply: 2)
12. very high salt concentration ?? - (reply: 4)
13. RNA electrophoresis - (reply: 2)
14. PCR product not migrating from wells...?? - (reply: 6)
15. How to determine gene knock-out from Agarose gel bands - (reply: 1)
16. An issue !! - (reply: 5)
17. What would be the adequate %gel/voltage/running time conditions for a ca. 320 kD - (reply: 3)
18. EMSA not detect a bindind - (reply: 7)
19. Visualization of DNA:RNA hybrid on TBE-UREA GEL - (reply: 8)
20. SDS page staning issue - (reply: 9)
21. All bands, including ladder, appear as double bands in EtBr stained gel - (reply: 6)
22. Forgot to wash the wells - (reply: 2)
23. Staining SDS-PAGE gel with EtBr? - (reply: 6)
24. DNA shows on Nanodrop but not on electrophoresis - (reply: 2)
25. Gel Bands - (reply: 1)
26. I want to separate two proteins having mw of 16.8 and 16.78 kDa. how can i accom - (reply: 2)
27. Sequencing gels equipment query - (reply: 2)
28. Electrophoresis Imaging - (reply: 1)
29. Electrophoresis after PCR : too many bands - (reply: 6)
30. Homogenous Cell Lysates - (reply: 1)

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