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Invitrogen™ Aladin Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA546705
Description
Peptide sequence: EHNNELVTGS SYESPPPDFR GQWINLPVLQ LTKDPLKTPG RLDHGTRTAF.
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.
Specifications
Aladin | |
Polyclonal | |
Unconjugated | |
AAAS | |
AAA; Aaas; AAASb; achalasia, adrenocortical insufficiency, alacrimia; achalasia, adrenocortical insufficiency, alacrimia (Allgrove, triple-A); ADRACALA; Adracalin; ALADIN; aladin WD repeat nucleoporin; Allgrove, triple-A; D030041N15Rik; GL003 | |
Rabbit | |
Affinity chromatography | |
RUO | |
8086 | |
-20°C, Avoid Freeze/Thaw Cycles | |
Liquid |
Western Blot | |
0.5 mg/mL | |
PBS with 2% sucrose and 0.09% sodium azide | |
Q9NRG9 | |
AAAS | |
Synthetic peptide directed towards the N-terminal of human AAAS (aa 20-69). | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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