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.
ALMS1
ALMS1, centrosome and basal body associated protein
Alstrom syndrome protein 1
:  ALSS Alstrom syndrome 1 Alstrom syndrome protein 1 KIAA0328
Product
Specifications
Ordering Information
Human
WB, IP, ICC, IF
Between 1200 and 1250
100
$339
$229
$99
Human
IP
Between 3400 and 3450
100
$339
$99
Human
100
Includes: 1 each of A301-815A and A301-816A
$472
Includes: 1 each of A301-815A and A301-816A
Human
ICC, IF
Between 1200 and 1250
100
$360
$99