Rabbit anti-ALMS1 Antibody Affinity Purified
Catalog #
ALMS1
Human
IP
Rabbit
Polyclonal
Whole IgG
between 3400 and 3450
IgG
Unconjugated
Antigen Affinity Purified
Product Details
Human
Human
2 - 8 °C
1 year from date of receipt
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.
Alternate Names
ALSS; Alstrom syndrome 1; Alstrom syndrome protein 1
Applications