SCFD1 Polyclonal Antibody, 20ul Live Cell Imaging disease:Defects in COL4A1 are a

disease:Defects in COL4A1 are a cause of brain small vessel disease with hemorrhage

ADAMTS18 (ADAM metallopeptidase with thrombospondin type 1 motif 18) encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family

a reduction in germ cell numbers

This gene appears to be an evolving pseudogene of L-threonine 3-dehydrogenase (TDH)

A mutation in this gene is the cause of autosomal dominant distal hereditary motor neuropathy type 2C

SCFD1 Polyclonal Antibody, 20ul Live Cell Imaging disease:Defects in COL4A1 are aInvolved in vesicular transport between the endoplasmic reticulum and the Golgi.,PTM: Phosphorylated upon DNA damage, probably by ATM or ATR.,Belongs to the STXBP unc 18 SEC1 family.,subunit: Binds STX5A.,