Phospho-Caldesmon (S759) Polyclonal Antibody, 20ul Roller Bottles Mutations in this gene are

Mutations in this gene are associated with Hirschsprung disease/Mowat-Wilson syndrome

2002 [PubMed 11784320])

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

Antibodies to 4

It is very similar to the family member HNRPH1

Phospho-Caldesmon (S759) Polyclonal Antibody, 20ul Roller Bottles Mutations in this gene areCALD1 (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