Mutations in this gene cause the X-linked Kallmann syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated and may have anti-protease activity.

WB 1:500 - 1:2000

A synthetic peptide corresponding to a sequence within amino acids 200-300 of human KAL1 (NP_000207.2).

Unmodified

Store at -20°. Avoid freeze / thaw cycles.