Strain specific CD94 expression analysis in heterozygous B-hCD94/hNKG2A/hNKG2C mice by flow cytometry. Splenocytes were collected from wild-type mice and heterozygous B-hCD94/hNKG2A/hNKG2C mice and stimulated with anti-CD3ε in vivo (7.5 μg/mice, stimulation for 24 hours, i.p. ), and analyzed by flow cytometry with species-specific anti-CD94 antibody. Human CD94 were exclusively detectable in heterozygous B-hCD94/hNKG2A/hNKG2C but not in wild-type mice.
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Strain specific NKG2A expression analysis in heterozygous B-hCD94/hNKG2A/hNKG2C mice by flow cytometry. Splenocytes were collected from wild-type mice and heterozygous B-hCD94/hNKG2A/hNKG2C mice and stimulated with anti-CD3ε in vivo (7.5 μg/mice, stimulation for 24 hours, i.p. ), and analyzed by flow cytometry with species-specific anti-NKG2A antibody. Human NKG2A were exclusively detectable in heterozygous B-hCD94/hNKG2A/hNKG2C but not in wild-type mice.
Strain specific NKG2C expression analysis in heterozygous B-hCD94/hNKG2A/hNKG2C mice by flow cytometry. Splenocytes were collected from wild-type mice and heterozygous B-hCD94/hNKG2A/hNKG2C mice and stimulated with anti-CD3ε in vivo (7.5 μg/mice, stimulation for 24 hours, i.p. ), and analyzed by flow cytometry with species-specific anti-NKG2C antibody. Human NKG2C were exclusively detectable in heterozygous B-hCD94/hNKG2A/hNKG2C mice but not in wild-type mice.