- Title
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Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons
- Authors
- England, S., Hilinski, W., de Jager, S., Andrzejczuk, L., Campbell, P., Chowdhury, T., Demby, C., Fancher, W., Gong, Y., Lin, C., Machikas, A., Rodriguez-Larrain, G., Roman Rivera, V., and Lewis, K.E.
- Source
Wild-Type. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: AGCCATTGCAAAACTTCACC. Reverse: AATTAACCCTCACTAAAGGGATGTGCCTTTTCTCATGCAAC. PCR product size: 1168 bp. |
mindbomb1ta52b mutant. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: AGCCATTGCAAAACTTCACC. Reverse: AATTAACCCTCACTAAAGGGATGTGCCTTTTCTCATGCAAC. PCR product size: 1168 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: AGCCATTGCAAAACTTCACC. Reverse: AATTAACCCTCACTAAAGGGATGTGCCTTTTCTCATGCAAC. PCR product size: 1168 bp. |
Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: ACAACATCCAGTGGCTAGGG. Reverse: AATTAACCCTCACTAAAGGGACGGAGACAGGCAGATAAAGC. PCR product size: 653 bp. Not spatially restricted. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: CATTCTGATGCTGTAACGACCAC. Reverse: AATTAACCCTCACTAAAGGGAAGCATCCCTTTGAGCTACAGTG. PCR product size: 975 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: ATCGAGAGCACACCCGACAAAAG. Reverse: AATTAACCCTCACTAAAGGGACACTAAGTGTTGAAGTGGAAGAGC. PCR product size: 457 bp. Embryos have been over-developed to detect all possible expression. EXPRESSION / LABELING:
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Wild-Type. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: GCGGTTCAAAAGACTTCAGC. Reverse: AATTAACCCTCACTAAAGGGATTCAGTTCTTGCAACAGACG. PCR product size: 897 bp. EXPRESSION / LABELING:
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mindbomb1ta52b mutant. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: GCGGTTCAAAAGACTTCAGC. Reverse: AATTAACCCTCACTAAAGGGATTCAGTTCTTGCAACAGACG. PCR product size: 897 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: GCGGTTCAAAAGACTTCAGC. Reverse: AATTAACCCTCACTAAAGGGATTCAGTTCTTGCAACAGACG. PCR product size: 897 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: TTTCTGTCCAACCCCTTCTG. Reverse: AATTAACCCTCACTAAAGGGATTGACCCCACACTGGCTATT. PCR product size: 905 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: CTGTCTGCAAAGCCACTCAC. Reverse: AATTAACCCTCACTAAAGGGACCTCTGCAGGCTACACATCTC. PCR product size: 641 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: GGATCAATCAGCAGCAGAGAAAC. Reverse: AATTAACCCTCACTAAAGGGAGGTCATCCTTTACATGCAGAGC. PCR product size: 1055 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: GGATCAATCAGCAGCAGAGAAAC. Reverse: AATTAACCCTCACTAAAGGGAGGTCATCCTTTACATGCAGAGC. PCR product size: 1055 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014, with the exception that the PCR annealing temperature was increased to 60oC. Primer sequences were: Forward: CCATCCACTCATCACGTGTC. Reverse: AATTAACCCTCACTAAAGGGACTTGCTTGTTAGGCCAGGAG. PCR product size: 873 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: CAAACGCGCAGACTATTTC. Reverse: AATTAACCCTCACTAAAGGGAGTTGTTGCGTAGGGGACACT. PCR product size: 1043 bp. EXPRESSION / LABELING:
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mindbomb1ta52b mutant. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: CAAACGCGCAGACTATTTC. Reverse: AATTAACCCTCACTAAAGGGAGTTGTTGCGTAGGGGACACT. PCR product size: 1043 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: CGGCAGTCTTCAGTAAGTTTGA. Reverse: AATTAACCCTCACTAAAGGGATGATGCTGTGTCATCACTGCT. PCR product size: 464 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: TCCATATCCTCCTCTTCCGACAG. Reverse: AATTAACCCTCACTAAAGGGATGTCATTGGTTCGTTCATCCTCAG. PCR product size: 817 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: TCCATATCCTCCTCTTCCGACAG. Reverse: AATTAACCCTCACTAAAGGGATGTCATTGGTTCGTTCATCCTCAG. PCR product size: 817 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: AGCTCATGCGTCTGGATAAC. Reverse: AATTAACCCTCACTAAAGGGAAAACGCCATTACCATTCAGG. PCR product size: 904 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: CGACGAAAACGAAGAGAAGG. Reverse: AATTAACCCTCACTAAAGGGAGTCCTCGAGCATCTGAAAGG. PCR product size: 925 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: GACTTCTGGCCTTGTTGAAGTG. Reverse: AATTAACCCTCACTAAAGGGATTTTCTGTCAAGGTTGTCAAGTC. PCR product size: 834 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: GACTTCTGGCCTTGTTGAAGTG. Reverse: AATTAACCCTCACTAAAGGGATTTTCTGTCAAGGTTGTCAAGTC. PCR product size: 834 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-15 (30 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: GACTTCTGGCCTTGTTGAAGTG. Reverse: AATTAACCCTCACTAAAGGGATTTTCTGTCAAGGTTGTCAAGTC. PCR product size: 834 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-25 (36 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: GACTTCTGGCCTTGTTGAAGTG. Reverse: AATTAACCCTCACTAAAGGGATTTTCTGTCAAGGTTGTCAAGTC. PCR product size: 834 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: ACACAGAACCCGTCCAGAAC. Reverse: AATTAACCCTCACTAAAGGGAGCGCTTTTAACCTCCAGATG. PCR product size: 883 bp. EXPRESSION / LABELING:
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mindbomb1ta52b mutant. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: ACACAGAACCCGTCCAGAAC. Reverse: AATTAACCCTCACTAAAGGGAGCGCTTTTAACCTCCAGATG. PCR product size: 883 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: ACACAGAACCCGTCCAGAAC. Reverse: AATTAACCCTCACTAAAGGGAGCGCTTTTAACCTCCAGATG. PCR product size: 883 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014, with the exception that in situ hybridization was performed at 65oC. Primer sequences were: Forward: TGTGGCAAAAGATTGTCAGG. Reverse: AATTAACCCTCACTAAAGGGACGTGCAACAAAGAGGTTTGA. PCR product size: 1019 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: ACATTGCTGGCAACCCTTAC. Reverse: aattaaccctcactaaagggaTCTTCCAGTGCCCAGTCTCT. PCR product size: 832 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: GTCAGTGGACGTGTGGTCAG. Reverse: AATTAACCCTCACTAAAGGGAAGCAAAAGGTGACACATCCA. PCR product size: 811 bp. No expression in the hindbrain. No expression in the spinal cord. EXPRESSION / LABELING:
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mindbomb1ta52b mutant. Prim-5 (24 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: GTCAGTGGACGTGTGGTCAG. Reverse: AATTAACCCTCACTAAAGGGAAGCAAAAGGTGACACATCCA. PCR product size: 811 bp. No expression in the hindbrain. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: GTCAGTGGACGTGTGGTCAG. Reverse: AATTAACCCTCACTAAAGGGAAGCAAAAGGTGACACATCCA. PCR product size: 811 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-10 (27 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: TGAATTTGCTGCTTCACAGG. Reverse: AATTAACCCTCACTAAAGGGACTCGAGAGTGGACCACCATTT. PCR product size: 1082 bp. EXPRESSION / LABELING:
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Wild-Type. Prim-15 (30 hpf). Probe synthesis and in situ hybridisation was performed as described in England et al., Identifying Transcription Factors Expressed by Ventral Spinal Cord Interneurons. ZFIN on-line publication, 2014. Primer sequences were: Forward: TGAATTTGCTGCTTCACAGG. Reverse: AATTAACCCTCACTAAAGGGACTCGAGAGTGGACCACCATTT. PCR product size: 1082 bp. EXPRESSION / LABELING:
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