Gene Expression Data
Assay Details
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Assay
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Reference:
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J:233299
Kamaludin AA, et al., Muscle dysfunction caused by loss of Magel2 in a mouse model of Prader-Willi and Schaaf-Yang syndromes. Hum Mol Genet. 2016 Sep 1;25(17):3798-3809
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Assay type:
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Immunohistochemistry
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MGI Accession ID:
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MGI:8275169
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Gene symbol:
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Dmd
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Gene name:
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dystrophin, muscular dystrophy
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Results
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Specimen
S5B WT:
postnatal adult
(more  )
Specimen
S5B WT:
(close  )
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Genetic Background:
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involves: C57BL/6J
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Age:
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postnatal adult
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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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Fresh Frozen
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Embedding:
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Cryosection
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Specimen
S5B Magel2:
(close )
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Genetic Background:
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C57BL/6-Magel2tm1Stw/J
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Mutant Allele(s):
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Magel2tm1Stw/Magel2tm1Stw
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Age:
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postnatal adult
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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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Fresh Frozen
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Embedding:
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Cryosection
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| Structure |
Level |
Pattern |
Image |
Note |
| TS28: gastrocnemius muscle |
Present |
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S5B Magel2 Dystrophin
,
S5B Magel2 Merge
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Expression similar between genotypes.
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Analysis Tools
