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DDI2 antibody

The Rabbit Polyclonal anti-DDI2 antibody has been validated for ELISA, WB and IHC. It is suitable to detect DDI2 in samples from Human and Mouse.
Catalog No. ABIN7246202

Quick Overview for DDI2 antibody (ABIN7246202)

Target

See all DDI2 Antibodies
DDI2 (DNA-Damage Inducible 1 Homolog 2 (DDI2))

Reactivity

Human, Mouse

Host

  • 24
Rabbit

Clonality

  • 24
Polyclonal

Conjugate

  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DDI2 antibody is un-conjugated

Application

  • 13
  • 12
  • 2
  • 2
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human DDI2

    Isotype

    IgG
  • Application Notes

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

    Restrictions

    For Research Use only
  • 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

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

    Alternative Name

    DDI2

    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
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