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SBDS antibody (AA 1-250)

The Mouse Monoclonal anti-SBDS antibody has been validated for WB, ELISA, IF and ICC. It is suitable to detect SBDS in samples from Human.
Catalog No. ABIN5775988

Quick Overview for SBDS antibody (AA 1-250) (ABIN5775988)

Target

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

Reactivity

  • 36
  • 16
  • 16
  • 7
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
Human

Host

  • 34
  • 2
Mouse

Clonality

  • 31
  • 5
Monoclonal

Conjugate

  • 19
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
This SBDS antibody is un-conjugated

Application

  • 18
  • 10
  • 8
  • 6
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)

Clone

AT1E8
  • Binding Specificity

    • 5
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    AA 1-250

    Purpose

    Human SBDS antibody

    Purification

    Purified

    Immunogen

    Recombinant human SBDS (1-250aa) purified from E. coli

    Isotype

    IgG2b kappa
  • Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    Phosphate-Buffered Saline ( pH 7.4) with 0.02 % Sodium Azide, 10 % glycerol

    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

    4 °C,-20 °C,-80 °C

    Storage Comment

    Can be stored at +2C to +8C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
  • Target

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

    Alternative Name

    SBDS

    Background

    The Shwachman-Bodian-Diamond syndrome (SBDS) is 249 amino acid ribosome maturation protein. The precise function of the SBDS protein is not known but it appears to play an important role in actin cytoskeletal function and mitotic spindle stabilization. Also, SBDS is required for the assembly of mature ribosomes and ribosome biogenesis. Mutations in the SBDS gene cause Shwachman-Diamond syndrome (SDS). SDS is an autosomal recessive disorder with clinical features that include pancreatic exocrine insufficiency, haematological dysfunction and skeletal abnormalities.

    NCBI Accession

    NP_057122

    Pathways

    Ribonucleoprotein Complex Subunit Organization, Ribosome Assembly
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