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. Author manuscript; available in PMC: 2010 Jun 1.
Published in final edited form as: Gen Comp Endocrinol. 2009 Mar 9;162(2):219–232. doi: 10.1016/j.ygcen.2009.03.001

Table 1.

Primer sequences used for Q-RT-PCR and in situ hybridization

Gene Symbol Presumed Process/Function Contig ID Strand Sequence Method
Epithelial Membrane Protein 1 EMP1 Proliferation/differentiation TC00532 F CTTGGCCATCATCTTTGG PCR
Epithelial Membrane Protein 1 EMP1 Proliferation/differentiation TC00532 R AAGAAGCGGCATCCTTTC PCR
Glutamate-ammonia Ligase GLUL Nitrogen metabolism TC00765 F ACTTTGGCGTTGTGGCTA PCR
Glutamate-ammonia Ligase GLUL Nitrogen metabolism TC00765 R TGGCTTCCGTGCTGTAGT PCR
Keratin 14 KRT14 Intermediate filament MC00279 F GCAGCTGACCGATTTGAG PCR
Keratin 14 KRT14 Intermediate filament MC00279 R CCAGCCGTGACTTGATGT PCR
Keratin 14 KRT14 Intermediate filament MC00279 F AATTAACCCTCACTAAAGGGAGATGCAGTCCCAACTGTCAATG ISH
Keratin 14 KRT14 Intermediate filament MC00279 R ATTTAGGTGACACTATAGAAGAGATCCAGCCAGGTGTTGGTAG ISH
Keratin 6A KRT6A Intermediate filament MC02467 F CCCTGCAGAAAGCCAAG PCR
Keratin 6A KRT6A Intermediate filament MC02467 R TGTCTAGGGCCAGCTTGA PCR
Keratin 6A KRT6A Intermediate filament MC02467 F AATTAACCCTCACTAAAGGGAGACGTTTGGATGGTGATCTGAG ISH
Keratin 6A KRT6A Intermediate filament MC02467 R ATTTAGGTGACACTATAGAAGAGTCCTGGTAGTCACGCAGTTG ISH
Matrix Metalloproteinase 1 MMP1 Collagen degradation MC01311 F CACCCGAAATCTGTGACAA PCR
Matrix Metalloproteinase 1 MMP1 Collagen degradation MC01311 R CGGCGCCAGAAGAATC PCR
Matrix Metalloproteinase 1 MMP1 Collagen degradation MC01311 F AATTAACCCTCACTAAAGGGAGACAGGAGCTCAGGGAAGAATG ISH
Matrix Metalloproteinase 1 MMP1 Collagen degradation MC01311 R ATTTAGGTGACACTATAGAAGAGAAGTGGACGTCTCCACCAAC ISH
Thyroid Hormone Receptor α TR-α Transcription factor N/A F GTCGGATGCCATCTTTGA PCR
Thyroid Hormone Receptor α TR-α Transcription factor N/A R CAGCACCGCCTGAAGTAG PCR
Thyroid Hormone Receptor β TR-β Transcription factor N/A F AACGCTGAATGGGGAAAT PCR
Thyroid Hormone Receptor β TR-β Transcription factor N/A R CGACATCCCAAGGTCAAA PCR
Uromodulin UMOD Protection/barrier MC01737 F GCGGATTCATTGACCATTC PCR
Uromodulin UMOD Protection/barrier MC01737 R TCGGAGTTGGTGATCTTGA PCR
Uromodulin UMOD Protection/barrier MC01737 F AATTAACCCTCACTAAAGGGAGATCCTGCTCCTACCCTCTCAA ISH
Uromodulin UMOD Protection/barrier MC01737 R ATTTAGGTGACACTATAGAAGAGGGTCACGGTGGACATTCTCT ISH
Calmodulin 2 CALM2 Ca regulation/signaling MC10283 F CCCGTATCTGCGTTTATCC PCR
Calmodulin 2 CALM 2 Ca regulation/signaling MC10283 R CTTAACGGAAGGTGGTTGG PCR
Calmodulin 2 CALM2 Ca regulation/signaling MC10283 F AATTAACCCTCACTAAAGGGAGAAAGGACTGGCTTGCAGTAGG ISH
Calmodulin 2 CALM2 Ca regulation/signaling MC10283 R ATTTAGGTGACACTATAGAAGAGAGGCATAACGCCAGCTAAGA ISH
Transcriptional Intermediary Factor 1 TIF1 Control gene MC00782 F CCTCTGGTCTCGGATCG PCR
Transcriptional Intermediary Factor 1 TIF1 Control gene MC00782 R TCCTGCGGAGGCTCTT PCR

PCR refers to Q-RT-PCR. Contig ID is the Sal-Site (www.ambystoma.org) identifier associated with each gene. Strand refers to the strand to which primer design was targeted. F = forward strand primer and R = reverse strand primer. Primers for TR-α and TR-β were designed from sequences obtained from the National Center for Biotechnology Information. For the “Contig ID” column, N/A implies that a gene does not have a Sal-Site contig ID.