Некатегоризовані сторінки

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  36. Cell engraftment index for SB623 was assessed using monoclonal human specific antibody (HuNu) that did not cross-react with rodent proteins
  37. 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
  38. 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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  46. Cells, therefore, have evolved a complicated proton transporting system to regulate cytosolic pH as well as the pH in other cellular compartments
  47. 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)
  48. Cells double-stained with antibodies to EOMES and T-bet; however, we could
  49. Cells double-stained with antibodies to EOMES and T-bet; on the other hand, we could
  50. Cells ended up harvested forty eight h afterwards and analyzed for Dies1 protein by Western blot utilizing anti-Flag antibody

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