MBIP1 Polyclonal Antibody, 50ul miRNA / siRNA Synthesis Defects in this gene are

Defects in this gene are also one of the causes of congenital stationary night blindness

Binds to CX3CR1

Mutations in this gene cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen)

This gene encodes one of the matrix-remodelling associated proteins

which is activated by binding of small GTPases such as CDC42 to an N-terminal regulatory domain

MBIP1 Polyclonal Antibody, 50ul miRNA / siRNA Synthesis Defects in this gene areInhibits the MAP3K12 activity to induce the activation of the JNK SAPK pathway.,subcellular location: Shows a cytoplasmic localization when co expressed with MAP3K12.,tissue specificity: Ubiquitous. High expression seen in the heart and lung.,