Fig. 10.
Fig. 10. Agarose gel electrophoresis of RT-PCR products stained with ethidium bromide. / (L) DNA ladder. (1) Bone marrow mononuclear cell mRNA with enolase primers showing an expected product of 329 bp. (2) mRNA from IL-2–activated NK cells with enolase primers. (3) Positive control of a 400-bp sequence of human SDF1a amplified with SDF1a primers. (4) mRNA from IL-2–activated NK cells with SDF1a primers showing an absence of SDF1a message. (5) Negative control, mRNA from IL-2–activated NK cells, reverse transcriptase was omitted. (6) Negative control, mRNA from activated NK cells was omitted. (7) Negative control, mRNA from activated NK cells, Taq polymerase omitted.

Agarose gel electrophoresis of RT-PCR products stained with ethidium bromide.

(L) DNA ladder. (1) Bone marrow mononuclear cell mRNA with enolase primers showing an expected product of 329 bp. (2) mRNA from IL-2–activated NK cells with enolase primers. (3) Positive control of a 400-bp sequence of human SDF1a amplified with SDF1a primers. (4) mRNA from IL-2–activated NK cells with SDF1a primers showing an absence of SDF1a message. (5) Negative control, mRNA from IL-2–activated NK cells, reverse transcriptase was omitted. (6) Negative control, mRNA from activated NK cells was omitted. (7) Negative control, mRNA from activated NK cells, Taq polymerase omitted.

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