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1. Co-localisation Analysis - immunofluorescence - (reply: 5)
2. black spots are found in cells and medium - (reply: 1)
3. Cell Membranes as an active barrier - (reply: 1)
4. Normalise cell count for protein analysis - (reply: 3)
5. Blockage of cadherin bindings of MCF-10A cells without harming hydrogels and cal - (reply: 2)
6. Should Lineage marker cocktail be used in cell lines to remove lineage specific - (reply: 1)
7. When overexpressing several genes using different vectors, what negative control - (reply: 2)
8. Transfection - (reply: 2)
9. The true monomers making RNA and DNA ? - (reply: 1)
10. Co-transfection of multiple plasmids - (reply: 1)
11. Culturing LoVo cells - (reply: 1)
12. Luciferase assay - experimental design - (reply: 1)
13. Cytotoxicity of hoechst staining in overnight experiment - (reply: 1)
14. Lentivirus packaging (no fluorescence) - (reply: 1)
15. exosome isolation - (reply: 1)
16. Synchronization of HEK293T cells for IP - (reply: 2)
17. About closing a Class II safety cabinet - (reply: 2)
18. Cell volume and reciprocal cell volume? Whaaat? - (reply: 1)
19. The adipose cell culturing - (reply: 2)
20. Migration Inhibitors - (reply: 1)
21. E-Cadherin Expression in OAW-42 Cells - (reply: 1)
22. Why HepG2 cells looked like that? - (reply: 2)
23. Cell death determination - (reply: 2)
24. Does anyone know of a stict S phase marker? - (reply: 2)
25. Jurkat cell - normal receptor/gene expressivity - (reply: 1)
26. GFP+ Transf. HEK293 GFP- in fluorescence microscopy? - (reply: 1)
27. Viral-Exososme Neutralization - (reply: 2)
28. control shRNA - (reply: 2)
29. Is any other method to maintain without changing media, or store cell culture fo - (reply: 2)
30. Does TritonX-100 lysis buffer break up mitochondrial membrane? - (reply: 2)
2. black spots are found in cells and medium - (reply: 1)
3. Cell Membranes as an active barrier - (reply: 1)
4. Normalise cell count for protein analysis - (reply: 3)
5. Blockage of cadherin bindings of MCF-10A cells without harming hydrogels and cal - (reply: 2)
6. Should Lineage marker cocktail be used in cell lines to remove lineage specific - (reply: 1)
7. When overexpressing several genes using different vectors, what negative control - (reply: 2)
8. Transfection - (reply: 2)
9. The true monomers making RNA and DNA ? - (reply: 1)
10. Co-transfection of multiple plasmids - (reply: 1)
11. Culturing LoVo cells - (reply: 1)
12. Luciferase assay - experimental design - (reply: 1)
13. Cytotoxicity of hoechst staining in overnight experiment - (reply: 1)
14. Lentivirus packaging (no fluorescence) - (reply: 1)
15. exosome isolation - (reply: 1)
16. Synchronization of HEK293T cells for IP - (reply: 2)
17. About closing a Class II safety cabinet - (reply: 2)
18. Cell volume and reciprocal cell volume? Whaaat? - (reply: 1)
19. The adipose cell culturing - (reply: 2)
20. Migration Inhibitors - (reply: 1)
21. E-Cadherin Expression in OAW-42 Cells - (reply: 1)
22. Why HepG2 cells looked like that? - (reply: 2)
23. Cell death determination - (reply: 2)
24. Does anyone know of a stict S phase marker? - (reply: 2)
25. Jurkat cell - normal receptor/gene expressivity - (reply: 1)
26. GFP+ Transf. HEK293 GFP- in fluorescence microscopy? - (reply: 1)
27. Viral-Exososme Neutralization - (reply: 2)
28. control shRNA - (reply: 2)
29. Is any other method to maintain without changing media, or store cell culture fo - (reply: 2)
30. Does TritonX-100 lysis buffer break up mitochondrial membrane? - (reply: 2)