Fig. 1.
Fig. 1. Inactivation of the murine CD24a (HSA) gene. (A) The promoter and first exon of the CD24a gene was replaced by a neomycin-resistance expression cassette in mouse embryonal stem cells by homologous recombination. (B) A Southern blot of EcoRI digested tail DNA was hybridized with a HincII-BamHI genomic DNA probe derived from the region immediately 5′ to the targeted replacement. Mice heterozygous for the mutation (+/−) show bands from both the intact allele (upper band) and the targeted allele. (C) Northern blots of total RNA extracted from the spleen and liver of both wild type (+/+) and HSA-deficient mice (-/-) was sequentially hybridized with HSA and glyceraldehyde phosphate dehydrogenase cDNA probes.

Inactivation of the murine CD24a (HSA) gene. (A) The promoter and first exon of the CD24a gene was replaced by a neomycin-resistance expression cassette in mouse embryonal stem cells by homologous recombination. (B) A Southern blot of EcoRI digested tail DNA was hybridized with a HincII-BamHI genomic DNA probe derived from the region immediately 5′ to the targeted replacement. Mice heterozygous for the mutation (+/−) show bands from both the intact allele (upper band) and the targeted allele. (C) Northern blots of total RNA extracted from the spleen and liver of both wild type (+/+) and HSA-deficient mice (-/-) was sequentially hybridized with HSA and glyceraldehyde phosphate dehydrogenase cDNA probes.

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