WDSUB1 Antikörper

Produktnummer ABIN7254652

Produktdetails anti-WDSUB1 Antikörper

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

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser WDSUB1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Antigen affinity purification

Immunogen: Synthetic peptide of human WDSUB1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000, ELISA 1:5000-1:10000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.7 mg/mL

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

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu WDSUB1

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

Andere Bezeichnung: WDSUB1 (WDSUB1 Produkte)

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

Hintergrund: 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.

Molekulargewicht:

Observed_MW: Refer to figures

Calculated_MW: 53 kDa

UniProt: Q8N9V3