Caldesmon Polyclonal Antibody, 50ul[BT-AP01118] Low-speed Centrifuges autosomal recessive craniometaphyseal dysplasia and

autosomal recessive craniometaphyseal dysplasia and heart malformations

high-quality polypropylene and feature a special hydrophobic inner surface treatment that significantly reduces sample loss

it does not stimulate ODC degradation

Mutations in this gene cause steroid-resistant nephrotic syndrome

It localizes to the outer membrane of mitochondria

Caldesmon Polyclonal Antibody, 50ul[BT-AP01118] Low-speed Centrifuges autosomal recessive craniometaphyseal dysplasia andCALD1 (caldesmon 1) encodes a calmodulin and actin binding protein that plays an essential role in the regulation of smooth muscle and nonmuscle contraction. The conserved domain of this protein possesses the binding activities to Ca(2+) calmodulin, actin, tropomyosin, myosin, and phospholipids. This protein is a potent inhibitor of the actin tropomyosin activated myosin MgATPase, and serves as a mediating factor for Ca(2+) dependent inhibition of