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Adracalin antibody

AAAS Reactivity: Human, Mouse WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7072884
  • Target See all Adracalin (AAAS) Antibodies
    Adracalin (AAAS) (Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))
    Reactivity
    • 31
    • 4
    • 2
    Human, Mouse
    Host
    • 27
    • 4
    Rabbit
    Clonality
    • 28
    • 3
    Polyclonal
    Conjugate
    • 17
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Adracalin antibody is un-conjugated
    Application
    • 31
    • 13
    • 13
    • 10
    • 5
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Cross-Reactivity
    Human
    Purification
    Affinity purification
    Immunogen
    Recombinant protein corresponding to Mouse Adracalin
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  • Application Notes
    WB (H,M) 1:500-1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % sodium azide
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
  • Target
    Adracalin (AAAS) (Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))
    Alternative Name
    Adracalin (AAAS Products)
    Synonyms
    zgc:85873 antibody, aladin antibody, Aladin antibody, AAA antibody, AAASb antibody, ADRACALA antibody, ADRACALIN antibody, ALADIN antibody, D030041N15Rik antibody, GL003 antibody, aladin WD repeat nucleoporin antibody, achalasia, adrenocortical insufficiency, alacrimia antibody, aladin WD repeat nucleoporin L homeolog antibody, Aaas antibody, aaas antibody, aaas.L antibody, AAAS antibody
    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.
    Molecular Weight
    60 kDa
    Gene ID
    223921
    NCBI Accession
    NP_700465
    UniProt
    P58742
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