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. Author manuscript; available in PMC: 2017 Nov 1.
Published in final edited form as: Wound Repair Regen. 2016 Oct 4;24(6):1004–1014. doi: 10.1111/wrr.12471

FIGURE 6. Detection of uniquely human genes in the PVA sponge model in hNSG mice.

FIGURE 6

RT-PCR was used for the detection of the expression of (A) uniquely human genes CHRFAM7A (Top row), TBC1D3 (middle row), and ARHGAP11B (bottom row) in hNSG mice from bone marrow (BM) and PVA sponge (PVA). Cells analyzed from NSG mice were used a negative control and primary human leukocytes cDNA (hCD45) used as a positive control. (B) Detection of human GAPDH in hNSG samples was a species specificity control, and detection of mouse GAPDH in all samples was a loading control.