ALMS1 Antibody

Mutations in the ALMS1 gene are the cause of Alstrom syndrome, a rare autosomal recessive disease characterized by type 2 diabetes mellitus, obesity, cardiomyopathy, and neurosensory defects such as cone-rod retinal dystrophy, and hearing loss. In the cell, ALMS1 localizes to basal bodies of ciliated cells and centrosomes and is thus a member of proteins associated with genetic ciliopathies.
    Product Specifications
    Catalog # Size Price
    ALMS1 AntibodyReactivity: Human
    Applications: WB, IP, ICC, IF
    Immunogen: Between 1200 and 1250
    A301-815A100 µl (0.2 mg/ml) $339Add to Cart
    A301-815A-M100 µl (10 blots) $229Add to Cart
    A301-815A-T20 µl (2 blots) $50Add to Cart
    ALMS1 AntibodyReactivity: Human
    Applications: IP
    Immunogen: Between 3400 and 3450
    A301-816A100 µl (1 mg/ml) $339Add to Cart
    A301-816A-T10 µl (1 mg/ml) $50Add to Cart

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