Сторінки без посилань

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Наступні сторінки не містять посилань на інші сторінки цієї вікі.

Нижче показано до 50 результати у діапазоні від #21 351 до #21 400.

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  19. Cell engraftment index for SB623 was assessed using monoclonal human specific antibody (HuNu) that did not cross-react with rodent proteins
  20. Cell lysates containing equal amounts of total proteins from wild type cells or cells transfected with scrambled, GRIM-19 or NDUFS3 siRNA were separated by SDS-polyacrylamide gel eletrophoresis
  21. Cell proliferation was performed by the cell viability assay. Six replicates for each group and the experiment repeated at least three times
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  29. Cells, therefore, have evolved a complicated proton transporting system to regulate cytosolic pH as well as the pH in other cellular compartments
  30. Cells compelled to spread in the existence of 500 kHz alternating electric fields exhibited an intermediate level of Septin localization to microtubules (Fig 3E and 3F)
  31. Cells double-stained with antibodies to EOMES and T-bet; however, we could
  32. Cells double-stained with antibodies to EOMES and T-bet; on the other hand, we could
  33. Cells ended up harvested forty eight h afterwards and analyzed for Dies1 protein by Western blot utilizing anti-Flag antibody
  34. Cells expressing the RhoA FRET biosensor were embedded in 3D ECM gels as before in the presence or absence of fibroblasts and activation measured
  35. Cells expressing vimentin had been drastically much more sensitive to WFA than those not expressing vimentin
  36. Cells expressing vimentin have been significantly a lot more sensitive to WFA than these not expressing vimentin
  37. Cells expressing vimentin have been significantly much more sensitive to WFA than these not expressing vimentin
  38. Cells expressing vimentin were substantially much more sensitive to WFA than these not expressing vimentin
  39. Cells from one lung per mouse were isolated, stained with Alexa-647 secondary antibody and quantified based on fluorescence
  40. Cells had been incubated with plasmid-Fugene mixture for 6 hours then media was replaced with fresh development medium and incubated for one more 24 hours
  41. Cells had been then treated with or devoid of PEITC
  42. Cells have been harvested at 72 hrs after an infection and detergent-soluble protein extracts have been analysed by densitometric examination of anti-gB TM immunoblots
  43. Cells have been incubated with plasmid-Fugene mixture for 6 hours after which media was replaced with fresh development medium and incubated for a further 24 hours
  44. Cells have been thawed, washed, and resuspended in stimulation buffer and 0.five mmol
  45. Cells have been then treated with or with out PEITC
  46. Cells show increased proinflammatory factor and decreased hematopoietic factor gene expression and enhance KOBA cell proliferation at the cost of supporting normal hematopoiesis
  47. Cells then knowledge aberrant mitotic exit, exhibit a G0/G1 block in mobile cycle development and apoptosis that is influenced by the cells' p53 mutational status
  48. Cells were being lysed in RIPA buffer, and proteins were being isolated from mobile lysates by immunoprecipitation as explained earlier
  49. Cells were pelleted and lysed in 100 mL of DMSO, and the absorbance at 550 nm was measured using a microplate reader
  50. Cells were placed in transwells and allowed to migrate for 4 h in the presence of vascular endothelial growth factor

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