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Top : New Forum Archives (2009-): : Molecular-Biology
1. Gel doubling banding and resolution problem - (reply: 1)
2. Can´t get rid of DNA contamination in RNA - (reply: 1)
3. PCR DNA bands too large on agarose gel - (reply: 1)
4. Easy to transfect primary cell line? - (reply: 1)
5. Sequence specific pulldown of dsDNA - (reply: 8)
6. Gene expression and transcription factors - (reply: 1)
7. RNA gel problem (melted bands) - (reply: 2)
8. RNA extraction and DNase treatment - (reply: 1)
9. Cloning purified PCR product into cells - (reply: 5)
10. Mention of Transgene Insertion into Cell Lines By Transfecting with cDNA - (reply: 2)
11. when to add polybrene for lentivirus transduction? - (reply: 1)
12. How to know the plasmid extracted are indeed the plasmid of interest? - (reply: 6)
13. In situ hybridization - (reply: 5)
14. Sypro Ruby Dye Front - (reply: 9)
15. Forced Expression vs. Enforced Expression - (reply: 1)
16. Co-immunoprecipitation non-specific binding - (reply: 2)
17. New webpage and software tools - (reply: 1)
18. What DCH5a cells are? / pCAMBIA1301 isolation from DHC5a cells - (reply: 3)
19. Can I snap freeze my tissue (liquid nitrogen) in Lysis buffer for later RNA extr - (reply: 6)
20. Gateway cloning not working. - (reply: 7)
21. Assays from very few number of cells - (reply: 1)
22. EM7 promoter - what is it? - (reply: 1)
23. Virus processing (filtration) of blood - How to? - (reply: 5)
24. TE buffer pH adjustment - (reply: 1)
25. Estimate cost for Molecular Docking software/devices - (reply: 1)
26. Polymorphism - (reply: 2)
27. PCR_QUALITY CONTROL - (reply: 2)
28. Difficult cloning/ligation/transformation blunt and sticky - (reply: 1)
29. TOP10F´ Chemically Competent E. coli - (reply: 1)
30. RNA purification with TRI_ low yield - (reply: 1)