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AAAS


Official Full Name
aladin WD repeat nucleoporin
Organism
Homo sapiens
Gene ID
8086
Background
The 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]
Synonyms
HB16; CREB2; TREB7; CREB-2; CRE-BP1

Cat.No. Product Name Price
AD00413Z Human AAAS adenoviral particles Inquiry
Cat.No. Product Name Price
SHH228506 shRNA set against Human AAAS (NM_015665.5) Inquiry
SHH228510 shRNA set against Mouse AAAS (NM_153416.2) Inquiry
SHH228514 shRNA set against Rat AAAS (NM_001106795.1) Inquiry
SHW018314 shRNA set against Danio rerio AAAS (NM_213225) Inquiry
Cat.No. Product Name Price
CDCB159218 Human AAAS ORF clone (BC000659) Inquiry
CDCB179789 Danio rerio AAAS ORF Clone (NM_213225) Inquiry
CDFH000004 Human AAAS cDNA Clone(NM_001173466.1) Inquiry
CDFR006523 Rat Aaas cDNA Clone(NM_001106795.1) Inquiry
CDCB183956 Rabbit AAAS ORF clone (XM_008256513.1) Inquiry
CDCR022604 Human AAAS ORF clone (NM_001173466.1) Inquiry
CDCR373534 Rat Aaas ORF Clone(NM_001106795.1) Inquiry
CDCS409034 Human AAAS ORF Clone (BC000659) Inquiry
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