A murine Mll-AF4 knock-in model results in lymphoid and myeloid deregulation and hematologic malignancy Blood Chen et al. 108: 669
Supplemental materials for: Chen et al
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Table S1. PCR primers (PDF, 43.2 KB) - 28-35 cycles of PCR was performed as follows: 94°C, 30sec; 60°C (55°C for HPRT), 30 sec; 72°C, 60sec. RT-PCR products were separated and visualized by 1.2% agarose gel.
Table S2. Relative expression levels of Mll fusion gene in young and diseased mice Mean (SD) detected by real time quantitative RT-PCR (PDF, 10.1 KB) - A two-way analysis of variance (two-way ANOVA) was used to evaluate possible differences in average expression levels from the two different fusion genes as well as the two age groups with the following results: 1) There is a difference between young mice and older mice (p<.01); the difference is larger among AF4 mice and smaller among AF9. This represents an “interaction” phenomenon (between age and type of gene). 2) Overall, there are no significance difference between Mll-AF4 and Mll-AF9 (p>.05). However, the result is masked by the above-mentioned interaction. The difference between AF4 and AF9 is marginally statistically significant among younger mice (p<.05) but not significant among older mice ― at least not with the small sample sizes to date.