NTAL Polyclonal Antibody, 20ul Custom Peptide Synthesis Mutations in this gene can

Mutations in this gene can cause optic atrophy 10| with or without ataxia| mental retardation| and seizures

and the PH domain interacts with phospholipids and is responsible for association of PSCDs with membranes

Designed with a flat cap and conical bottom

Basigin encoded by BSG is a plasma membrane protein that is important in spermatogenesis

Mutations in this gene have been implicated in autosomal dominant Alzheimer disease and cerebroarterial amyloidosis (cerebral amyloid angiopathy)

NTAL Polyclonal Antibody, 20ul Custom Peptide Synthesis Mutations in this gene canThis gene is one of the contiguous genes at 7q11. 23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein.