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Fig. 3

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ZDB-IMAGE-160822-14
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Figures for Shen et al., 2002
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Fig. 3

Expression of zneo1 splice variants in zebrafish. (a) Schematic representation of RT-PCRs used for alternative splicing study. RT-PCR was performed with the indicated primers: znsp1, TCACGCACAGACCATCAAAG; znsp1′, TGGTCTTCCAACGCACTGTA; znsp2, CTGTAGTGAGCAAAGAGG; znsp2′, AGGTCTGGTGGTTTGAGA; znsp3, GGGCAACTCCAAAGATCTCAA; znsp3′, TGAAAGGTCAGTGGTGCAAGA under standard conditions. The resulting products derived from the first strand cDNAs of various adult tissues and staged embryos were subsequently cloned and sequenced. The possible splice isoforms are illustrated in the figure and named after the region amplified and the presence or absence of the alternative splices. FN4-FN6, fibronectin type III domains 4-6; hpf, hours post-fertilization; sp1-sp4, alternative splice 1-4 (indicated by dotted lines); TM, transmembrane domain. (b) Expression of zneo1 splice variants in adult and embryonic zebrafish.

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Reprinted from Mechanisms of Development, 118(1-2), Shen, H., Illges, H., Reuter, A., and Stürmer, C., Cloning, expression, and alternative splicing of neogenin1 in zebrafish, 219-223, Copyright (2002) with permission from Elsevier. Full text @ Mech. Dev.