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RAX2 Rabbit Polyclonal Antibody, 20ul Lysosome The protein encoded by this

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RAX2 Rabbit Polyclonal Antibody, 20ul Lysosome The protein encoded by thisThis gene encodes a homeodomain containing protein that plays a role in eye development. Mutation of this gene causes age related macular degeneration type 6 an eye disorder resulting in accumulations of protein and lipid beneath the retinal pigment epithelium and within the Bruch's membrane. Defects in this gene can also cause cone rod dystrophy type 11 a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in

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Description

The protein encoded by this gene is highly similar to S

SSTR2 (somatostatin receptor 2) is a member of the superfamily of receptors having seven transmembrane segments and is expressed in highest levels in cerebrum and kidney

which houses over 700 genes and comprises nearly 3% of the human genome

The protein forms a ternary complex with insulin-like growth factor acid-labile subunit (IGFALS) and either insulin-like growth factor (IGF) I or II

and functions as a negative regulator of cell migration and adhesion triggered by the beta-2 integrin signal transduction pathway

RAX2 Rabbit Polyclonal Antibody, 20ul Lysosome The protein encoded by thisThis gene encodes a homeodomain containing protein that plays a role in eye development. Mutation of this gene causes age related macular degeneration type 6 an eye disorder resulting in accumulations of protein and lipid beneath the retinal pigment epithelium and within the Bruch's membrane. Defects in this gene can also cause cone rod dystrophy type 11 a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in

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