Bethyl will be closed Monday, May 28th in observance of Memorial Day and will resume normal business hours on Tuesday, May 29th. Thank you!

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
$339
$229
$99
Human
IP
Between 3400 and 3450
$339
$99
Human
WB, IP, ICC-IF
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
$360
$99