MMP13 Rabbit pAb
产品介绍
Defects in MMP13 are the cause of spondyloepimetaphyseal dysplasia Missouri type (SEMD-MO) [MIM:602111]. A bone disease characterized by moderate to severe metaphyseal changes, mild epiphyseal involvement, rhizomelic shortening of the lower limbs with bowing of the femora and/or tibiae, coxa vara, genu varum and pear-shaped vertebrae in childhood. Epimetaphyseal changes improve with age.
产品性质
应用案例
稀释比 WB: 1/500-1/1000 IHC: 1/50-1/100
存储条件
冰袋运输,-20℃保存。
COA
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