Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

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

BBS5 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN973755
  • Target Alle BBS5 Produkte
    BBS5 (Bardet-Biedl Syndrome 5 (BBS5))
    Protein Region
    Middle Region
    Spezies
    Human
    Quelle
    • 3
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Produktmerkmale
    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.
    Aufreinigung
    Purified
  • Applikationshinweise
    Each Investigator should determine their own optimal working dilution for specific applications.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Konzentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handhabung
    Avoid repeated freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    BBS5 (Bardet-Biedl Syndrome 5 (BBS5))
    Synonyme
    zgc:56578 Peptide, 1700049I01Rik Peptide, 2700023J09Rik Peptide, Bardet-Biedl syndrome 5 Peptide, Bardet-Biedl syndrome 5 (human) Peptide, bbs5 Peptide, BBS5 Peptide, Bbs5 Peptide
    Hintergrund
    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
    Molekulargewicht
    39 kDa
    Gen-ID
    129880
    NCBI Accession
    NM_152384, NP_689597
    UniProt
    Q8N3I7
Sie sind hier:
Kundenservice