Gene Expression Data
Assay Details
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Assay
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Reference:
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J:166923
Wang B, et al., Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B. Hum Mol Genet. 2011 Jan 15;20(2):271-85
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Assay type:
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RT-PCR
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MGI Accession ID:
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MGI:5755250
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Gene symbol:
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Msx2
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Gene name:
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msh homeobox 2
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Probe:
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Msx2-pS, Msx2-pT
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Probe preparation:
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labelled with SYBR green
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Assay notes:
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This assay is a quantitative RT-PCR. Gapdh was used as the standard.
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Results
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Image: 5E Msx2
Notes:
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Analysis Tools
