Adracalin anticorps (AA 320-516)

N° du produit ABIN1886368

Détail du produit anti-Adracalin anticorps

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

Épitope: AA 320-516

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Adracalin est non-conjugé

Application: Western Blotting (WB)

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 320 and 516 of Human AAAS

Information d'application

Indications d'application: Suggested dilutions:
Western blotting: 1.500-1.3000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: Biohazard Informations: This product contains thimerosal which is hazardous.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Détails sur Adracalin

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

Autre désignation: Aladin (AAAS Produits)

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

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.[provided by RefSeq]

Poids moléculaire: 60 kDa

ID gène: 8086

NCBI Accession: NM_015665, NP_056480