Adracaline (AAAS) (NM 015665) Humaan Recombinant Proteïne

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]

Purified recombinant protein of Human achalasia, adrenocortical insufficiency, alacrimia (AAAS), transcript variant 1, Glu322-End, with N-terminal His tag, expressed in E. coli, 50ug

AAA; AAASb; ADRACALA; ADRACALIN; ALADIN; GL003

8086

Q9NRG9

NM_015665

12q13.13

E. coli

N-His

>50 ug/mL as determined by microplate BCA method

> 80% as determined by SDS-PAGE and Coomassie blue staining

Liquid

50mM Tris, 8M Urea, pH8.0.

24.1 kDa

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.

AAAS

Human

NP_056480

https://www.ncbi.nlm.nih.gov/gene/8086

https://www.uniprot.org/uniprot/Q9NRG9

https://www.ncbi.nlm.nih.gov/nuccore/NM_015665

https://www.ncbi.nlm.nih.gov/nuccore/NP_056480