AAAS monoclonal Antibody | MB62002

AAAS monoclonal Antibody | MB62002 | Gentaur UK, US & Europe Distribution

Host: Mouse

Reactivity: Human, Mouse, Rat

Application: IHC, WB

Application Range: WB 1:2000, IHC 1:150

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. [provided by RefSeq, Mar 2010]

Storage & Stability: PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Specificity: aladin WD repeat nucleoporin

Molecular Weight: 59.4 kDa (Predicted)

Note: For research use only, not for use in diagnostic procedure.

Alternative Names: AAA; AAASb; ADRACALA; ADRACALIN; ALADIN; GL003

Immunogen: Human recombinant protein fragment corresponding to amino acids 322-546 of human AAAS (NP_056480) produced in E.coli.

Conjugate: Unconjugated

Modification: Unmodification

Purification & Purity: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)

Pathway: N/A