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/Catalog #SpecificationsPrice
    ALMS1 Antibody
    A301-815A
    Reactivity: Human
    Applications: WB, IP, ICC, IF
    $314.00
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    ALMS1 Antibody
    A301-816A
    Reactivity: Human
    100% Sequence Identity:
    Applications: IP
    $314.00
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    ALMS1 Antibody AbVantage™ Pack
    A310-647A
    Applications: WB, IP, ICC, IF
    Reactivity: Human
    Quantity: 1 each of A301-815A and A301-816A
    $437.00
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    ALMS1 IHC Antibody
    IHC-00367
    Applications: ICC, IF
    Reactivity: Human
    Quantity: 0.1 ml (50 - 250 slides)
    $360.00
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