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AAAS
Aladin WD repeat nucleoporinThe protein encoded by this gene 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. The encoded protein is part of the nuclear pore complex and is anchored there by NDC1. Defects in this gene are a cause of achalasia-addisonianism-alacrima syndrome (AAAS), also called triple-A syndrome or Allgrove syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]
Top validated antibodies |
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| Proteintech Group |  15127-1-AP |
1 references | Polyclonal |
WB
EL
ICC
IHC
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| LSBio | LS-C335665 |
Polyclonal |
WB
ICC
IHC
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| antibodies-online | ABIN396498 |
5 references | Monoclonal |
WB
EL
IHC
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| Novus Biologicals | NBP2-21596 |
1 references | Polyclonal |
WB
ICC
IHC
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| Atlas Antibodies | HPA040086 |
Polyclonal |
WB
ICC
IHC
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