Gene Expression Data
Assay Details
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Assay
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Reference:
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J:71941
Baumgart E, et al., Mitochondrial alterations caused by defective peroxisomal biogenesis in a mouse model for Zellweger syndrome (PEX5 knockout mouse). Am J Pathol. 2001 Oct;159(4):1477-94
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Assay type:
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Immunohistochemistry
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MGI Accession ID:
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MGI:7378394
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Gene symbol:
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Ndufa9
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Gene name:
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NADH:ubiquinone oxidoreductase subunit A9
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Results
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Specimen
4E:
embryonic day 18.5
(more  )
Specimen
4E:
(close  )
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Genetic Background:
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involves: 129S1/Sv * 129X1/SvJ
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Age:
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embryonic day 18.5
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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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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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| Structure |
Cell Type |
Level |
Pattern |
Image |
Note |
| TS26: liver |
hepatocyte |
Present |
Regionally restricted |
4E
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Expression in mitochondria.
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Specimen
4F:
(close )
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Genetic Background:
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involves: 129S1/Sv * 129X1/SvJ
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Mutant Allele(s):
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Pex5tm1Baes/Pex5tm1Baes
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Age:
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embryonic day 18.5
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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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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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| Structure |
Cell Type |
Level |
Pattern |
Image |
Note |
| TS26: liver |
hepatocyte |
Weak |
Non-Uniform |
4F
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Reduction of overall expression intensity, strongest for complex I. Marked intercellular heterogeneity in distribution of expression compared to wildtype.
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Analysis Tools
