DDI2 anticorps

N° du produit ABIN7246202

Détail du produit anti-DDI2 anticorps

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DDI2 est non-conjugé

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

Attributs du produit: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogène: Fusion protein of human DDI2

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000, IHC 1:50-1:300, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1.32 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 DDI2

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

Autre désignation: DDI2 (DDI2 Produits)

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

Sujet: 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.

Poids moléculaire:

Observed_MW: Refer to figures

Calculated_MW: 45 kDa

UniProt: Q5TDH0