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DDX39B antibody

This anti-DDX39B antibody is a Rabbit Polyclonal antibody detecting DDX39B in IHC and IF. Suitable for Human, Mouse and Rat.
Catalog No. ABIN7264385

Quick Overview for DDX39B antibody (ABIN7264385)

Target

See all DDX39B Antibodies
DDX39B (DEAD (Asp-Glu-Ala-Asp) Box Polypeptide 39B (DDX39B))

Reactivity

  • 33
  • 8
  • 6
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 28
  • 5
Rabbit

Clonality

  • 26
  • 7
Polyclonal

Conjugate

  • 16
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DDX39B antibody is un-conjugated

Application

  • 23
  • 17
  • 16
  • 5
  • 4
  • 3
  • 3
  • 1
  • 1
Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human DDX39B (NP_004631.1).

    Isotype

    IgG
  • Application Notes

    IHC 1:100-1:200 IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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

    DDX39B (DEAD (Asp-Glu-Ala-Asp) Box Polypeptide 39B (DDX39B))

    Alternative Name

    DDX39B

    Background

    This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13 kDa, V1 subunit G2) gene.

    Gene ID

    7919

    UniProt

    Q13838

    Pathways

    Ribonucleoprotein Complex Subunit Organization
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