GTD2B Rabbit Polyclonal Antibody, 100ul Pipette Controller Type IV collagen proteins are

Type IV collagen proteins are integral components of basement membranes

Diseases associated with CSGALNACT1 include bell's palsy

Mutations in CYP1B1 have been associated with primary congenital glaucoma

Mutations in DOK7 are a cause of familial limb-girdle myasthenia autosomal recessive

this protein is likely involved in hair formation and spermatogenesis in human as well

GTD2B Rabbit Polyclonal Antibody, 100ul Pipette Controller Type IV collagen proteins areThis gene encodes a glycosylated phosphoprotein with a leucine zipper motif two helix loop helix motifs (I repeats) that are similar to domains found in the TFII I family of transcription factors one CHARLIE8 transposable element like sequence and a BED zinc finger. This gene lies within a region that is deleted in Williams Beuren syndrome. Alternatively spliced variants which encode different protein isoforms have been described; however not all