GPTC8 Polyclonal Antibody, 100ul Pathway and Network Analysis Mutations in this gene cause

Mutations in this gene cause complement component 5 deficiency

Measure IL-6 levels with precision and uncover groundbreaking data

ADAM17 (ADAM metallopeptidase domain 17) encodes a member of the ADAM (a disintegrin and metalloprotease domain) family

blood coagulation

EPHB2 encodes a member of the Eph receptor family of receptor tyrosine kinase transmembrane glycoproteins

GPTC8 Polyclonal Antibody, 100ul Pathway and Network Analysis Mutations in this gene causeThe protein encoded by this gene contains an RNA processing domain, a zinc finger domain, a lysine rich region and a serine rich region. A mutation in the serine rich region of the protein is thought to be associated with hyperuricemia (PMID: 21594610). Alternative splicing results in multiple transcript variants encoding different isoforms.