奇异不良素(DYSF)检测试剂盒FER1L1; LGMD2B
; Dysferlin,Limb Girdle Muscular Dystrophy 2B(Autosomal Recessive); Fer-1-like protein 1; Dystrophy-associated fer-1-like protein- ￥800 - 1300
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- 2025年07月07日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
100
- 供应商：
南京赛泓瑞
- 应用：
酶联法样本检测
- 适应物种：
人/大鼠/小鼠等各类物种
- 样本：
血清 细胞等
- 规格：
48T/96T
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文献和实验Molecular Investigation of LGMD2B-Haplotype Analysis and Mutation Screening
The limb-girdle muscular dystrophies (LGMDs) are generally characterized by weakness and atrophy of the proximal muscles. In 1994, the authors localized a form of autosomal recessive LGMD (LGMD2B) to chromosome 2p13 (1 ). Patients with LGMD2
Molecular Analysis of p94 and Its Application to Diagnosis of Limb Girdle Muscular Dystrophy Type 2A
p94 (also called calpain 3, nCL-1, or CAPN3) is a calpain large subunit homologue, which is predominantly expressed in skeletal muscle (1 –4 ). The mRNA level of p94 in skeletal muscle is at least 10 times higher
Limb-girdle muscular dystrophy 9LGMD) type 2A (LGMD2A; MIM253600) is an autosomal recessive disorder belonging to the group of progressive MDs. LGMD2A is characterized by symmetrical atrophy of the pelvic, scapular, and trunk muscles
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