CD58 Polyclonal Antibody, 100ul[BT-AP01563] Recombinant Ab Production Deficiencies lead to the skeletal

Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia

This gene is located in a cluster on chromosome 10 with five other closely related genes

Related pseudogenes have been defined on the X chromosome

A gene mutation

Sulfotransferases (e

CD58 Polyclonal Antibody, 100ul[BT-AP01563] Recombinant Ab Production Deficiencies lead to the skeletalCD93 molecule encoded by CD93 is a cell surface glycoprotein and type I membrane protein that was originally identified as a myeloid cell specific marker. The encoded protein was once thought to be a receptor for C1q, but now is thought to instead be involved in intercellular adhesion and in the clearance of apoptotic cells. The intracellular cytoplasmic tail of this protein has been found to interact with moesin, a protein known to play a role in