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A-Z / ALMS1
 

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 is also known as KIAA0328 and ALSS.
 
Product / Catalog #SpecificationsPrice
ALMS1 Antibody
A301-815A		Applications: WB, IP
Reactivity: Human
Quantity: 0.1 ml (20 - 100 blots)
$280.00
Data Sheet
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ALMS1 Antibody
A301-816A		Applications: IP
Reactivity: Human
Quantity: 0.1 ml
$280.00
Data Sheet
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ALMS1 Antibody AbVantage™ Pack
A310-647A		Applications: WB, IP
Reactivity: Human
Quantity: 1 each of A301-815A and A301-816A
$390.00
Data Sheet
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ALMS1 IHC Antibody
IHC-00367		Applications: ICC-IF
Reactivity: Human
Quantity: 0.1 ml (50 - 250 slides)
$360.00
Data Sheet
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ALMS1 Blocking Peptide
BP301-815		Applications: Blocks A301-815A
Quantity: 50 mcg
$115.00
Data Sheet
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ALMS1 Blocking Peptide
BP301-816		Applications: Blocks A301-816A
Quantity: 50 mcg
$115.00
Data Sheet
Add to Cart
 
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