Fig. 2.
Fig. 2. SHIP deletion. (A) The two bands produced using the 2666-3247 primer set, shown in Fig 1B, were subcloned and sequenced. The larger (581 bp) band corresponds to the published SHIP sequence. The smaller (398 bp) band has a deletion of 183 nucleotides at the site shown, but is otherwise identical. (B) SHIP genomic DNA was isolated from a lambda genomic DNA library. Phage clones which hybridized with the 581 bp product of the 2666-3247 PCR primers were sequenced to show the NPXY-containing exon. Exon sequence is in upper case letters, and the sequence of the ▵183 deletion is in bold type. The verified splice acceptor and donor are shown in shaded boxes, and the potential splice sites that would produce the ▵183 deletion as an intron are shown in open boxes. Numbering refers to the SHIP cDNA sequence as in Fig 1.

SHIP deletion. (A) The two bands produced using the 2666-3247 primer set, shown in Fig 1B, were subcloned and sequenced. The larger (581 bp) band corresponds to the published SHIP sequence. The smaller (398 bp) band has a deletion of 183 nucleotides at the site shown, but is otherwise identical. (B) SHIP genomic DNA was isolated from a lambda genomic DNA library. Phage clones which hybridized with the 581 bp product of the 2666-3247 PCR primers were sequenced to show the NPXY-containing exon. Exon sequence is in upper case letters, and the sequence of the ▵183 deletion is in bold type. The verified splice acceptor and donor are shown in shaded boxes, and the potential splice sites that would produce the ▵183 deletion as an intron are shown in open boxes. Numbering refers to the SHIP cDNA sequence as in Fig 1.

Close Modal

or Create an Account

Close Modal
Close Modal