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SBDS antibody (AA 19-241)

The Rabbit Polyclonal anti-SBDS antibody is suitable to detect SBDS in samples from Human, Mouse and Rat. It has been validated for WB, ELISA, IF and FACS.
Catalog No. ABIN7871577
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for SBDS antibody (AA 19-241) (ABIN7871577)

Target

See all SBDS Antibodies
SBDS (Shwachman-Bodian-Diamond Syndrome (SBDS))

Reactivity

  • 39
  • 17
  • 17
  • 7
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
Human, Mouse, Rat

Host

  • 36
  • 3
Rabbit

Clonality

  • 31
  • 8
Polyclonal

Conjugate

  • 22
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
This SBDS antibody is un-conjugated

Application

  • 21
  • 10
  • 9
  • 7
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)
  • Binding Specificity

    • 5
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    AA 19-241

    Purpose

    SBDS Antibody / Shwachman-Bodian-Diamond syndrome protein

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids R19-D241) was used as the immunogen for the SBDS antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the SBDS antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the SBDS antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    SBDS (Shwachman-Bodian-Diamond Syndrome (SBDS))

    Alternative Name

    SBDS

    Background

    Ribosome maturation protein SBDS is a protein that in humans is encoded by the SBDS gene. This gene encodes a highly conserved protein that plays an essential role in ribosome biogenesis. The encoded protein interacts with elongation factor-like GTPase 1 to disassociate eukaryotic initiation factor 6 from the late cytoplasmic pre-60S ribosomal subunit allowing assembly of the 80S subunit. Mutations within this gene are associated with the autosomal recessive disorder Shwachman-Bodian-Diamond syndrome. This gene has a closely linked pseudogene that is distally located.

    UniProt

    Q9Y3A5

    Pathways

    Ribonucleoprotein Complex Subunit Organization, Ribosome Assembly
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