Dmd-Q995X

모델명

C57BL/6Smoc-Dmdem1(Q995X)Smoc

카탈로그

NM-KI-18026

모델 상태

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유전자 요약

Official Symbol
Dmd

모델 설명

These mice carry a p.Q995X mutation in Dmd gene.

Disease Connection

Duchenne muscular dystrophy

검증 데이터

dmd-1.png

Fig1 Mouse dystrophin expression is abolished due to the p.Q995X mutation.

mdx.png

Fig2 Histopathology of WT and MDX mice(male, 6-month-old) muscle showing less uniform muscle fibers with inflammation and clustered nuclei.

mdx-2.png

Fig3 Limb grip strength tests in MDX mice.

The assessment of limb strength in experimental mice were performed by means of grip strength meter (BIO-G53, Bioseb, France). The mice were allowed to grab the pull bar and are then gently pulled backwards. The force applied to the bar just before it loses grip was recorded as peak resistance force (expressed in grams). To reduced procedure-related variability, the tests were repeated 4 to 5 times and the average was recorded.


당신은 또한 좋아할 수 있습니다

Shanghai Model Organisms Center Inc has licensed CRISPR-Cas9 technology from Broad Institute

On Dec 16, 2018, Broad Institute and Shanghai Model Organisms Center Inc (SMOC) has entered into a non-exclusive license agreement under which Broad has granted SMOC worldwide rights to commercialize a service platform for genetically modified mouse models under Broad's intellectual property.

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Milestones

Our vision is to provide researchers all over the world with comprehensive, convenient and professional animal model services to facilitate a simplified and highly-efficient approach towards uncovering the mysteries of life.

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