Background:

Mutations in KAL1 cause the X-linked Kallmann syndrome. Anosmin-1 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.

Classification:

Primary antibody

Alternative names:

KAL1; ADMLX; KAL; KALIG1; Anosmin-1; Adhesion molecule-like X-linked; Kallmann syndrome protein

Species reactivity:

Human

Host:

Rabbit

Isotype:

IgG

Immunogen:

The antiserum was produced against synthesized peptide derived from human KAL1. AA range:151-200

Concentration:

1 mg/ml

Molecular weight:

76112

Applications:

WB, ELISA

Storage:

-20°C for one year

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