UBA1 Polyclonal Antibody, 20ul Molecular Sciences and heterozygous deletion of the

and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype

CCBP2 is expressed in a range of tissues and hemopoietic cells

The encoded protein is an actin-binding protein that is activated by the serine/threonine kinase Akt and plays a role in cytoskeleton remodeling and cell migration

Among its related pathways are Axon guidance

• Advance features include speed/RCF switch

UBA1 Polyclonal Antibody, 20ul Molecular Sciences and heterozygous deletion of theUbiquitin like modifier activating enzyme 1 encoded by UBA1 catalyzes the first step in ubiquitin conjugation to mark cellular proteins for degradation. This gene complements an X linked mouse temperature sensitive defect in DNA synthesis, and thus may function in DNA repair. It is part of a gene cluster on chromosome Xp11. 3. Alternatively spliced transcript variants that encode the same protein have been described.