Gene Expression Data
Assay Details
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Assay
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Reference:
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J:160674
Mai S, et al., The missense mutation W290R in Fgfr2 causes developmental defects from aberrant IIIb and IIIc signaling. Dev Dyn. 2010 Jun;239(6):1888-900
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Assay type:
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Immunohistochemistry
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MGI Accession ID:
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MGI:5574512
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Gene symbol:
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Runx2
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Gene name:
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runt related transcription factor 2
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Antibody:
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anti-Runx2 (S-19): sc-12488
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Detection system:
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Biotinylated secondary antibody/[Strept]avidin coupled to horseradish peroxidase
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Results
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Specimen
2G:
embryonic day 16.5
(more  )
Specimen
2G:
(close  )
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Genetic Background:
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Not Specified
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Age:
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embryonic day 16.5
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Sex:
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Not Specified
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Type:
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section
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Embedding:
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Paraffin
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Specimen
2H:
embryonic day 16.5; \ Fgfr2m1Sgg/\Fgfr2 +
(more )
Specimen
2H:
(close )
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Genetic Background:
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involves: C3H/HeJ * C57BL/6J
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Mutant Allele(s):
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\Fgfr2m1Sgg/\Fgfr2+
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Age:
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embryonic day 16.5
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Sex:
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Not Specified
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Type:
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section
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Embedding:
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Paraffin
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Specimen
2I:
(close )
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Genetic Background:
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involves: C3H/HeJ * C57BL/6J
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Mutant Allele(s):
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\Fgfr2m1Sgg/\Fgfr2m1Sgg
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Age:
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embryonic day 16.5
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Sex:
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Not Specified
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Type:
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section
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Embedding:
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Paraffin
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| Structure |
Level |
Pattern |
Image |
Note |
| TS24: cranium |
Present |
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2I
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The number of positive cells is reduced in this mutant.
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Analysis Tools
