Anti-AAAS Aptamer SELEX Service(Cat#: CTApt-883)

This is an aptamer development services to screening aptamers binds to the AAAS with an affinity of 1nM~1μM.

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3’ Modification
 
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Certificate of Analysis Lookup

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Summary

Specifications
Target Category Protein
Target AAAS
Alternative Names Aladin WD Repeat Nucleoporin; Aladin; Achalasia, Adrenocortical Insufficiency, Alacrimia; Allgrove, Triple-A; Adracalin; ADRACALA; Achalasia, Adrenocortical Insufficiency, Alacrimia (Allgrove, Triple-A) ; ADRACALIN; ALADIN; AAASb; GL003; AAAS; AAA
Gene ID 8086
UniProt ID Q9NRG9
Target Overview 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.
Chemical Modification N/A
Type DNA
Length 20-80 nt
Affinity (Kd) 1nM~1μM
Binding Conditions/Buffer PBS; buffer system with Serum; other
For Research Use Only. Not for Diagnostic or Therapeutic Applications.
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