Table 3.

Expression of protected p16 exon 2 fragment in polycythemia vera and normal erythroid colony-forming cells

Exp no.Normal ECFCsPV ECFCsp16 density, healthy donorsp16 density, patients with PV% increase in PV
N7  1 073   
  PV3  17 044 1 590 
  PV6  5 863 550 
 N9  1 437   
  PV4  5 834 410 
  PV5  15 275 1 063 
N11  731   
  PV1  6 085 845 
N2  630   
  PV2  2 668 283 
N13  3 319   
  PV8  16 173 387 
N12  2 290   
  PV9  8 300 362 
N8  1 225   
  PV7  3 478 284 
N14  1 280   
  PV10  3 625 283 
 N15  651   
  PV11  3 707 439 
Exp no.Normal ECFCsPV ECFCsp16 density, healthy donorsp16 density, patients with PV% increase in PV
N7  1 073   
  PV3  17 044 1 590 
  PV6  5 863 550 
 N9  1 437   
  PV4  5 834 410 
  PV5  15 275 1 063 
N11  731   
  PV1  6 085 845 
N2  630   
  PV2  2 668 283 
N13  3 319   
  PV8  16 173 387 
N12  2 290   
  PV9  8 300 362 
N8  1 225   
  PV7  3 478 284 
N14  1 280   
  PV10  3 625 283 
 N15  651   
  PV11  3 707 439 

The density of p16 exon 2 assayed by RNase protection assay was quantified with a laser scanning densitometer and normalized to the amount of the total RNA present in the lane by comparison with the housekeeping gene mRNA. The percentage increase in patients with PV was obtained using the density in PV divided by the normal control density in the same gel so that all conditions were the same.

ECFCs indicates erythroid colony-forming cells; PV, polycythemia vera.

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