DDI2 Polyclonal Antibody
€0.00
In stock
SKU
E-AB-52572
Catalog Number: E-AB-52572
Isotype: Rabbit IgG
Reactivity: human, mouse
Applications: IHC,ELISA
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse
Applications: IHC,ELISA
Datasheet, Questions? Contact us!
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.
Research Area: Cell Biology
Synonyms:
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
Immunogen: Fusion protein of human DDI2
Swissprot: Q5TDH0
Gene Accession: BC006011
Purification Method: Antigen affinity purification
Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4
Concentration: 0.84 mg/mL
Dilution: IHC 1:50-1:300, ELISA 1:5000-1:10000
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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.
Research Area: Cell Biology
Synonyms:
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
Immunogen: Fusion protein of human DDI2
Swissprot: Q5TDH0
Gene Accession: BC006011
Purification Method: Antigen affinity purification
Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4
Concentration: 0.84 mg/mL
Dilution: IHC 1:50-1:300, ELISA 1:5000-1:10000
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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