Adracalin 抗体
(Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))
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].
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38 results
AAAS
适用: 人
WB, IF (cc), IF (p)
宿主: 兔
Polyclonal
AbBy Fluor® 750
Latest Publications for our Adracalin 抗体
: "Nuclear pore heterogeneity influences HIV-1 infection and the antiviral activity of MX2." in: eLife, Vol. 7, (2019) (PubMed).Aliases for Adracalin 抗体
aladin WD repeat nucleoporin (Aaas) 抗体achalasia, adrenocortical insufficiency, alacrimia (aaas) 抗体
aladin WD repeat nucleoporin L homeolog (aaas.L) 抗体
aladin WD repeat nucleoporin (AAAS) 抗体
aladin WD repeat nucleoporin (aaas) 抗体
achalasia, adrenocortical insufficiency, alacrimia (Aaas) 抗体
AAA 抗体
AAASb 抗体
ADRACALA 抗体
ADRACALIN 抗体
aladin 抗体
Aladin 抗体
ALADIN 抗体
D030041N15Rik 抗体
GL003 抗体
zgc:85873 抗体
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