Background:

This gene encodes a lysyl oxidase| which likely functions as an amine oxidase and plays a role in the formation of crosslinks in collagens and elastin. Deletion of the related gene in mouse causes neonatal mortality with cleft palate| spine deformity| and defects in collagen organization. A mutation in this gene was found in a family with Stickler syndrome.

Classification:

Primary antibody

Alternative names:

LOXL3

Species reactivity:

Human, Mouse

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human LOXL3

Concentration:

1 mg/ml

Molecular weight:

82830

Applications:

WB

Storage:

-20°C for 1 year

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