Adracalin (AAAS) (NM_015665) Human Recombinant Protein
Product Specifications
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]
Synonyms
AAA; AAASb; ADRACALA; ADRACALIN; ALADIN; GL003
Gene ID
8086
UniProt
Q9NRG9
Accession Number mRNA
NM_015665
Chromosomal Location
12q13.13
Expression System
Sf9
Tag
C-DDK
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
50mM Tris-HCl, pH8.0, 100mM glycine, 10% glycerol.
Molecular Weight
59.4 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
AAAS
Species
Human
Protein ID
NP_056480
Overview
Purified recombinant protein of Human achalasia, adrenocortical insufficiency, alacrimia (AAAS), transcript variant 1, full length, with C-terminal DDK tag, expressed in sf9, 20ug
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/8086
Uniprot URL
https://www.uniprot.org/uniprot/Q9NRG9
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_015665
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_056480
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