HTRA1 Polyclonal Antibody, 100ul Nucleic Acid Amplification The Gerbich and Yus phenotypes

The Gerbich and Yus phenotypes are due to deletion of exon 3 and 2

This eosinophil-specific chemokine is thought to be involved in eosinophilic inflammatory diseases such as atopic dermatitis

results in a flash of light that decays rapidly

Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC)

Ammonium transporter Rh type A encoded by RHAG is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane

HTRA1 Polyclonal Antibody, 100ul Nucleic Acid Amplification The Gerbich and Yus phenotypesThis gene encodes a member of the trypsin family of serine proteases. This protein is a secreted enzyme that is proposed to regulate the availability of insulin like growth factors (IGFs) by cleaving IGF binding proteins. It has also been suggested to be a regulator of cell growth. Variations in the promoter region of this gene are the cause of susceptibility to age related macular degeneration type 7.