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Animal Model >> null >> M_MECP2_1_CKO_HE Construct Details |
| Model Details :M_MECP2_1_CKO_HE
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Model Type |
Genetic
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Model Genotype |
Homozygous
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Mutation |
Conditional deletion of exon 3 which encodes most of the methyl-CpG-binding domain of Mecp2 using Nestin-cre, in neuronal, glial and other cell types in the central and peripheral nervous system, in male mice |
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Allele Type |
Conditional loss-of-function |
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Strain of Origin |
129/Sv |
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Genetic Background |
Not Specified |
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ES Cell Line |
129/Sv, B6129F1 |
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Mutant ES Cell Line |
Not Specified |
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Model Source |
Not Specified |
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Reference |
Chen RZ , et al. 2001
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