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Bardet-Biedl Syndrome 5 (BBS5) (Middle Region) Peptide

BBS5 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN973755
  • Target See all BBS5 products
    BBS5 (Bardet-Biedl Syndrome 5 (BBS5))
    Protein Region
    Middle Region
    Origin
    Human
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-BBS5 antibody (Catalog #: ARP52931_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Purification
    Purified
  • Application Notes
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    BBS5 (Bardet-Biedl Syndrome 5 (BBS5))
    Synonyms
    zgc:56578 Peptide, 1700049I01Rik Peptide, 2700023J09Rik Peptide, Bardet-Biedl syndrome 5 Peptide, Bardet-Biedl syndrome 5 (human) Peptide, bbs5 Peptide, BBS5 Peptide, Bbs5 Peptide
    Background
    BBS5 is a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is required for the formation of cilia.This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is required for the formation of cilia. Alternate transcriptional splice variants have been observed but have not been fully characterized.

    Alias Symbols: -

    Protein Size: 341
    Molecular Weight
    39 kDa
    Gene ID
    129880
    NCBI Accession
    NM_152384, NP_689597
    UniProt
    Q8N3I7
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