Adracalin Protein (DYKDDDDK Tag)

Produktnummer ABIN2714524

Produktdetails

Target: Adracalin (AAAS) (Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))

Protein-Typ: Recombinant

Spezies: Human

Quelle: Insect cells (Sf9)

Aufreinigungstag / Konjugat: Dieses Adracalin Protein ist gelabelt mit DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human Aladin (full length, C-term DDK tag, transcript variant 1) protein expressed in Sf9 cells.
• Produced with end-sequenced ORF clone

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

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 50 mM Tris-HCl, pH 8.0, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: Adracalin (AAAS) (Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))

Andere Bezeichnung: Aladin (AAAS Produkte)

Synonyme: zgc:85873 Protein, aladin Protein, Aladin Protein, AAA Protein, AAASb Protein, ADRACALA Protein, ADRACALIN Protein, ALADIN Protein, D030041N15Rik Protein, GL003 Protein, aladin WD repeat nucleoporin Protein, achalasia, adrenocortical insufficiency, alacrimia Protein, aladin WD repeat nucleoporin L homeolog Protein, Aaas Protein, aaas Protein, aaas.L Protein, AAAS Protein

Hintergrund: 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.

Molekulargewicht: 59.4 kDa

NCBI Accession: NP_056480