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Adracalin antibody
This Rabbit Polyclonal antibody specifically detects Adracalin in WB, ELISA, IHC and IF. It exhibits reactivity toward Human, Mouse and Rat.
Quick Overview for Adracalin antibody (ABIN7111183)
Target
See all Adracalin (AAAS) Antibodies
Adracalin (AAAS)
(Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))
Reactivity
All reactivities for Adracalin antibodies
Human, Mouse, Rat
Host
All hosts for Adracalin antibodies
Rabbit
Clonality
All clonalities for Adracalin antibodies
Polyclonal
Conjugate
All conjugates for Adracalin antibodies
This Adracalin antibody is un-conjugated
Application
All applications for Adracalin antibodies
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)
Product Details anti-Adracalin Antibody
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Purification
Immunogen affinity purified
Purity
≥95 % as determined by SDS-PAGE
Immunogen
achalasia, adrenocortical insufficiency, alacrimia (Allgrove, triple-A)
Isotype
IgG
Alternatives
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Application Details
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Application Notes
WB: 1:500 - 1:2000, IHC: 1:50 - 1:200, IF: 1:50 - 1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,
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
Storage Comment
-20°C for 12 months (Avoid repeated freeze / thaw cycles.)
Expiry Date
12 months
Target Details for Adracalin
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Target
Adracalin (AAAS)
(Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))
Alternative Name
ALADIN
Background
Synonyms:AAA, AAAS, AAASb, ADRACALA, ADRACALIN, ALADIN, DKFZp586G1624, GL003 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. Two transcript variants encoding different isoforms have been found for this gene.
Molecular Weight
60 kDa
Gene ID
8086
UniProt
Q9NRG9
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