DDI2 Antikörper

Produktnummer ABIN7246202

Produktdetails anti-DDI2 Antikörper

Target: DDI2 (DNA-Damage Inducible 1 Homolog 2 (DDI2))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DDI2 Antikörper ist unkonjugiert

Applikation: ELISA, Western Blotting (WB), Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Antigen affinity purification

Immunogen: Fusion protein of human DDI2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000, IHC 1:50-1:300, ELISA 1:5000-1:10000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1.32 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 DDI2

Target: DDI2 (DNA-Damage Inducible 1 Homolog 2 (DDI2))

Andere Bezeichnung: DDI2 (DDI2 Produkte)

Synonyme: RP4-680D5.5 antikoerper, 1110056G13Rik antikoerper, 1700027M01Rik antikoerper, 9130022E05Rik antikoerper, AI604911 antikoerper, AU040698 antikoerper, zgc:63515 antikoerper, DNA damage inducible 1 homolog 2 antikoerper, DNA-damage inducible protein 2 antikoerper, DNA damage inducible 1 homolog 2 L homeolog antikoerper, DDI2 antikoerper, Ddi2 antikoerper, ddi2 antikoerper, ddi2.L antikoerper

Hintergrund: DDI1 and DDI2 are ubiquitin receptor homologs of the Saccharomyces cerevisiae ddi1 protein, which is involved in regulation of the cell cycle and the late secretory pathway. DDI2 is a 399 amino acid protein that contains one ubiquitin-like domain and exists as three isoforms as a result of alternative splicing. The gene encoding DDI2 maps to human chromosome 1, the largest human chromosome which spans about 260 million base pairs and makes up 8 % of the human genome. Other notable genes located on chromosome 1 include LMNA, which is associated with the rare aging disease Hutchinson-Gilford progeria, and the MUTYH gene, which is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome.

Molekulargewicht:

Observed_MW: Refer to figures

Calculated_MW: 45 kDa

UniProt: Q5TDH0