Rabbit anti-Aladin Antibody Affinity Purified
Catalog #
Aladin
Human
,Mouse
IHC
,IP
,WB
Rabbit
Polyclonal
Whole IgG
Between 496 and C-terminus
IgG
Unconjugated
Antigen Affinity Purified
Product Details
Mouse,
Human
Human
Human
2 - 8 °C
1 year from date of receipt
USA
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)].
Alternate Names
AAA; AAASb; achalasia, adrenocortical insufficiency, alacrimia; ADRACALA; ADRACALIN; ALADIN; Allgrove, triple-A; GL003
Applications