WDSUB1 anticorps

N° du produit ABIN7254652

Détail du produit anti-WDSUB1 anticorps

Antigène: WDSUB1 (WD Repeat, Sterile alpha Motif and U-Box Domain Containing 1 (WDSUB1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WDSUB1 est non-conjugé

Application: Western Blotting (WB), ELISA

Attributs du produit: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogène: Synthetic peptide of human WDSUB1

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.7 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur WDSUB1

Antigène: WDSUB1 (WD Repeat, Sterile alpha Motif and U-Box Domain Containing 1 (WDSUB1))

Autre désignation: WDSUB1 (WDSUB1 Produits)

Synonymes: anticorps WDSUB1, anticorps 1700048E19Rik, anticorps 2610014F08Rik, anticorps zgc:154085, anticorps ubox6, anticorps wdsam1, anticorps UBOX6, anticorps WDSAM1, anticorps WD repeat, sterile alpha motif and U-box domain containing 1, anticorps WD repeat, SAM and U-box domain containing 1, anticorps WD repeat, sterile alpha motif and U-box domain containing 1 S homeolog, anticorps WDSUB1, anticorps wdsub1, anticorps Wdsub1, anticorps wdsub1.S

Sujet: WDSUB1 (WD repeat, SAM and U-box domain-containing protein 1), also known as UBOX6 or WDSAM1, is a 476 amino acid protein that contains one SAM (sterile alpha motif) domain, one U-box domain and seven WD repeats. Existing as two isoforms due to alternative splicing, WDSUB1 is encoded by a gene located on chromosome 2. The second largest human chromosome, chromosome 2 encodes over 1,400 genes and comprises nearly 8 % of the human genome, housing a number of disease-associated genes. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes. Additionally, an extremely rare recessive genetic disorder, Alstrm syndrome, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.

Poids moléculaire:

Observed_MW: Refer to figures

Calculated_MW: 53 kDa

UniProt: Q8N9V3