S26A7 Rabbit Polyclonal Antibody, 100ul Culture Plate Inserts an autosomal recessive skeletal disorder

an autosomal recessive skeletal disorder

involved in the respective process

along with GTP

This gene has also been identified as a co-activator of HIF1A (hypoxia-inducible factor 1 alpha)

and also initiates signaling events within the platelet that lead to enhanced platelet activation

S26A7 Rabbit Polyclonal Antibody, 100ul Culture Plate Inserts an autosomal recessive skeletal disorderThis gene is one member of a family of sulfate anion transporter genes. Family members are well conserved in gene structure and protein length yet have markedly different tissue expression patterns. This gene has abundant and specific expression in the kidney. Alternatively spliced transcript variants that encode different isoforms have been described.