Fig. 7.
Fig. 7. KIR expressing p210+ NK92 cells derive from the same clone. / In a Southern blot analysis, genomic DNA from parental, eGFP+, and p210-eGFP+(p210+) NK92 cells was digested withEcoRI, electrophoresed on a 0.7% agarose gel, and probed with a 32P-eGFP probe. Representative lanes show that CD158b/j+/CD158e− (lane 4), CD158b/j+/CD158e+ (lane 5), and CD158b/j−/CD158e− (lane 6) p210+NK92 cell populations express identical dominant bands, indicating that they derive from the same clone. KIR-negative eGFP+ NK92 cells show a smear (lane 1), and 2 different p210+ clones show a different unique band (lanes 2-3).

KIR expressing p210+ NK92 cells derive from the same clone.

In a Southern blot analysis, genomic DNA from parental, eGFP+, and p210-eGFP+(p210+) NK92 cells was digested withEcoRI, electrophoresed on a 0.7% agarose gel, and probed with a 32P-eGFP probe. Representative lanes show that CD158b/j+/CD158e (lane 4), CD158b/j+/CD158e+ (lane 5), and CD158b/j/CD158e (lane 6) p210+NK92 cell populations express identical dominant bands, indicating that they derive from the same clone. KIR-negative eGFP+ NK92 cells show a smear (lane 1), and 2 different p210+ clones show a different unique band (lanes 2-3).

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