Figure 2
Figure 2. TNF-α expression in B6.GT mice. (A) RNA was purified from 106 FACS sort-purified murine spleen IgM+ B cells, CD3+ conventional T cells, or IgM−CD3+B220+ DN T cells, or from peritoneal exudate cells (PEC), for assessment of TNF-α, TRAIL, FasL, and GAPDH mRNA levels by conventional semiquantitative RT-PCR. Data shown are representative of 2 independently repeated PCR analyses for each mRNA. (B) Serum TNF-α protein assessed by ELISA assay and quantitated relative to a recombinant murine TNF-α as a standard, with the limit of detection of TNF-α protein of approximately 10 pg/mL (line). Data shown are representative of an independently repeated TNF-α ELISA.

TNF-α expression in B6.GT mice. (A) RNA was purified from 106 FACS sort-purified murine spleen IgM+ B cells, CD3+ conventional T cells, or IgMCD3+B220+ DN T cells, or from peritoneal exudate cells (PEC), for assessment of TNF-α, TRAIL, FasL, and GAPDH mRNA levels by conventional semiquantitative RT-PCR. Data shown are representative of 2 independently repeated PCR analyses for each mRNA. (B) Serum TNF-α protein assessed by ELISA assay and quantitated relative to a recombinant murine TNF-α as a standard, with the limit of detection of TNF-α protein of approximately 10 pg/mL (line). Data shown are representative of an independently repeated TNF-α ELISA.

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