DDI2 Polyclonal Antibody

DDI2

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.

PBS with 0.05% NaN3 and 40% Glycerol,pH7.4

45 kDa

1.32 mg/mL

Unconjugated

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

Fusion protein of human DDI2

Refer to figures

Antigen affinity purification

DDI1 DNA damage inducible 1 homolog 2;Ddi2;DDI2;DNA damage inducible 1 homolog 2 (S. cerevisiae);DNA damage inducible 1 homolog 2;DNA damage inducible protein 2;MGC14844;Protein DDI1 homolog 2;RP4-680D5.5

Q5TDH0