Aladin Antibody

Aladin is a member of the WD-repeat family of regulatory proteins and may be involved in normal development of the peripheral and central nervous system. Aladin is part of the nuclear pore complex and is anchored there by NDC1. Defects in the coding gene are a cause of achalasia-addisonianism-alacrima syndrome (AAAS), also called triple-A syndrome or Allgrove syndrome [taken from NCBI Entrez Gene (Gene ID: 8086)].
AAAS
aladin WD repeat nucleoporin
Aladin
:  AAA AAASb achalasia, adrenocortical insufficiency, alacrimia achalasia, adrenocortical insufficiency, alacrimia (Allgrove, triple-A) ADRACALA adracalin aladin Allgrove, triple-A GL003
Product
Specifications
Ordering Information
Human, Mouse
WB, IP, IHC-P
Between 496 to 546
$339
$229
$99