DDI2 antibody

Catalog No. ABIN7246202

Product Details anti-DDI2 Antibody

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

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DDI2 antibody is un-conjugated

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

Characteristics: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogen: Fusion protein of human DDI2

Isotype: IgG

Application Details

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

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1.32 mg/mL

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

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for DDI2

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

Alternative Name: DDI2 (DDI2 Products)

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

Background: 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.

Molecular Weight:

Observed_MW: Refer to figures

Calculated_MW: 45 kDa

UniProt: Q5TDH0