Phospho-Caldesmon (S759) Polyclonal Antibody, 20ul Roller Bottles Heterozygous loss-of-function mutations in KLF1

Heterozygous loss-of-function mutations in KLF1 result in the dominant In (Lu) blood phenotype

ATP6AP2 encodes a protein that is associated with adenosine triphosphatases (ATPases)

usually increasing in size when transmitted to successive generations

Hirschsprung disease type 2

Phospho-Caldesmon (S759) Polyclonal Antibody, 20ul Roller Bottles Heterozygous loss-of-function mutations in KLF1CALD1 (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