Adracalin Protein (DYKDDDDK Tag)
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- Antigène Voir toutes Adracalin (AAAS) Protéines
- Adracalin (AAAS) (Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))
- Type de proteíne
- Recombinant
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Origine
- Humain
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Source
- Insect cells (Sf9)
- Purification/Conjugué
- Cette Adracalin protéine est marqué à la DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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- Recombinant human Aladin (full length, C-term DDK tag, transcript variant 1) protein expressed in Sf9 cells.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product AAAS Protéine
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- Indications d'application
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 50 mM Tris-HCl, pH 8.0, 100 mM glycine, 10 % glycerol.
- Stock
- -80 °C
- Stockage commentaire
- 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.
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- Antigène
- Adracalin (AAAS) (Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))
- Autre désignation
- Aladin (AAAS Produits)
- Synonymes
- 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
- Sujet
- 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.
- Poids moléculaire
- 59.4 kDa
- NCBI Accession
- NP_056480
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