PJVK Rabbit Polyclonal Antibody, 100ul Shaker&Mixing Mutations in HSD3B7 are associated

Mutations in HSD3B7 are associated with a congenital bile acid synthesis defect which leads to neonatal cholestasis

involved in vesicular fusion and trafficking

Hole edge design to prevent cross contamination

ATP6AP2 encodes a protein that is associated with adenosine triphosphatases (ATPases)

Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes

PJVK Rabbit Polyclonal Antibody, 100ul Shaker&Mixing Mutations in HSD3B7 are associatedThe protein encoded by this gene is a member of the gasdermin family a family which is found only in vertebrates. The encoded protein is required for the proper function of auditory pathway neurons. Defects in this gene are a cause of non syndromic sensorineural deafness autosomal recessive type 59 (DFNB59).