Fig. 5.
Fig. 5. PCR-screening of YAC contig between markers D10S191 and D10S548. (A) The inferred position of the cubilin gene (designatedCUB) between D10S1661 and WI-5445. The individual YACs and their genetic marker content (x) are arranged essentially as in the Whitehead WC10.1 contig. (B) Agarose gels aligned to the individual YAC clones, with CUB-specific PCR fragments corresponding to YACs 956a7 and 917b1. The bottom lane is genomic test DNA. The incorrectly sized PCR fragment in lane 721g12 is scored as negative (see text).

PCR-screening of YAC contig between markers D10S191 and D10S548. (A) The inferred position of the cubilin gene (designatedCUB) between D10S1661 and WI-5445. The individual YACs and their genetic marker content (x) are arranged essentially as in the Whitehead WC10.1 contig. (B) Agarose gels aligned to the individual YAC clones, with CUB-specific PCR fragments corresponding to YACs 956a7 and 917b1. The bottom lane is genomic test DNA. The incorrectly sized PCR fragment in lane 721g12 is scored as negative (see text).

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