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Adracalin antibody (N-Term)
This anti-Adracalin antibody is a Rabbit Polyclonal antibody detecting Adracalin in WB. Suitable for Human.
Quick Overview for Adracalin antibody (N-Term) (ABIN5516315)
Target
See all Adracalin (AAAS) Antibodies
Adracalin (AAAS)
(Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))
Reactivity
All reactivities for Adracalin antibodies
Human
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)
Product Details anti-Adracalin Antibody
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Binding Specificity
All epitopes for Adracalin antibodies
N-Term
Sequence
EHNNELVTGS SYESPPPDFR GQWINLPVLQ LTKDPLKTPG RLDHGTRTAF
Characteristics
This is a rabbit polyclonal antibody against AAAS. It was validated on Western Blot.
Purification
Affinity Purified
Immunogen
The immunogen is a synthetic peptide directed towards the N-terminal region of Human AAAS
Alternatives
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Application Details
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Application Notes
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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
For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
Target Details for Adracalin
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Target
Adracalin (AAAS)
(Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))
Alternative Name
AAAS
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. Alias Symbols: AAAS, ADRACALA, GL003, Protein Interaction Partner: UBC, SUMO1, NEDD8, REL, ISG15, Protein Size: 546
Gene ID
8086
NCBI Accession
NP_056480
UniProt
Q9NRG9
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