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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
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$457.98
$538.80
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Quick Overview for BUD31 antibody (ABIN7246052)

Target

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

Reactivity

  • 56
  • 31
  • 22
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Rat, Mouse

Host

  • 52
  • 4
Rabbit

Clonality

  • 44
  • 12
Polyclonal

Conjugate

  • 29
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
This BUD31 antibody is un-conjugated

Application

  • 35
  • 19
  • 18
  • 10
  • 7
  • 5
  • 2
  • 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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