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BUD31 antibody

The Rabbit Polyclonal anti-BUD31 antibody has been validated for WB, ELISA and IHC. It is suitable to detect BUD31 in samples from Human, Rat and Mouse.
Catalog No. ABIN7246052

Quick Overview for BUD31 antibody (ABIN7246052)

Target

See all BUD31 Antibodies
BUD31 (BUD31 Homolog (BUD31))

Reactivity

  • 45
  • 29
  • 21
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Rat, Mouse

Host

  • 41
  • 4
Rabbit

Clonality

  • 42
  • 3
Polyclonal

Conjugate

  • 27
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
This BUD31 antibody is un-conjugated

Application

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  • 10
  • 6
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Full length fusion protein

    Isotype

    IgG
  • Application Notes

    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.5 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

    BUD31 (BUD31 Homolog (BUD31))

    Alternative Name

    BUD31

    Background

    BUD31 (Protein G10 homolog, EDG-2) is a 144 amino acid protein encoded by the human gene BUD31. BUD31 is a nuclear protein that belongs to the BUD31 (G10) family. BUD31 is found on chromosome 7 which is about 158 milllion bases long, encodes over 1,000 genes and makes up about 5 % of the human genome. Chromosome 7 has been linked to osteogenesis imperfecta, Pendred syndrome, lissencephaly, citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the long (q) arm of human chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 17 kDa

    UniProt

    P41223
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