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AAAS Monoclonal Antibody (OTI7H7), TrueMAB™, OriGene

Mouse Monoclonal Antibody
Supplier: OriGene TA808617

Description
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
AAAS | |
Monoclonal | |
Unconjugated | |
AAAS | |
AAA, AAASb, ADRACALA, ADRACALIN, ALADIN, GL003 | |
Mouse | |
Affinity Chromatography | |
RUO | |
8086 | |
-20° C, Avoid Freeze/Thaw Cycles | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot | |
OTI7H7 | |
PBS with 1% BSA, 50% glycerol and 0.02% sodium azide | |
Q9NRG9 | |
AAAS | |
Human recombit protein fragment corresponding to amino acids 322-546 of human AAAS produced in E.coli. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG2a |
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