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BBS10 Antikörper (C-Term)

Der Kaninchen Polyklonal Anti-BBS10-Antikörper wurde für WB und FACS validiert. Er ist geeignet, BBS10 in Proben von Human zu detektieren.
Produktnummer ABIN651074

Kurzübersicht für BBS10 Antikörper (C-Term) (ABIN651074)

Target

Alle BBS10 Antikörper anzeigen
BBS10 (Bardet-Biedl Syndrome 10 (BBS10))

Reaktivität

  • 41
  • 2
  • 1
  • 1
Human

Wirt

  • 40
  • 1
Kaninchen

Klonalität

  • 41
Polyklonal

Konjugat

  • 13
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser BBS10 Antikörper ist unkonjugiert

Applikation

  • 31
  • 15
  • 13
  • 13
  • 8
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), Flow Cytometry (FACS)

Klon

RB24715
  • Bindungsspezifität

    • 15
    • 7
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 515-544, C-Term

    Aufreinigung

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This BBS10 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 515-544 amino acids from the C-terminal region of human BBS10.

    Isotyp

    Ig Fraction
  • Applikationshinweise

    WB: 1:1000. FC: 1:10~50

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Haltbarkeit

    6 months
  • Target

    BBS10 (Bardet-Biedl Syndrome 10 (BBS10))

    Andere Bezeichnung

    BBS10

    Hintergrund

    BBS10 is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by progressive retinal degeneration, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene is likely not a ciliary protein but rather has distant sequence homology to type II chaperonins. As a molecular chaperone, this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes.

    Molekulargewicht

    80838

    Gen-ID

    79738

    NCBI Accession

    NP_078961

    UniProt

    Q8TAM1
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