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Invitrogen™ Aladin Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA550308
Description
The antibody detects endogenous levels of total Aladin protein.
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 | |
Antigen affinity chromatography | |
RUO | |
8086 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot | |
1 mg/mL | |
PBS with 40% glycerol and 0.05% sodium azide; pH 7.4 | |
Q9NRG9 | |
AAAS | |
Fusion protein corresponding to residues near the C terminal of human achalasia, adrenocortical insufficiency, alacrimia. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
Safety and Handling
WARNING: Cancer - www.P65Warnings.ca.gov
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