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BBS2 Antikörper

BBS2 Reaktivität: Maus, Ratte WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7263435
  • Target Alle BBS2 Antikörper anzeigen
    BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
    Reaktivität
    • 11
    • 5
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Maus, Ratte
    Wirt
    • 8
    • 3
    Kaninchen
    Klonalität
    • 10
    • 1
    Polyklonal
    Konjugat
    • 11
    Dieser BBS2 Antikörper ist unkonjugiert
    Applikation
    • 11
    • 4
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human BBS2 (NP_114091.3).
    Isotyp
    IgG
    Top Product
    Discover our top product BBS2 Primärantikörper
  • Applikationshinweise
    WB 1:500-1:2000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
    Andere Bezeichnung
    BBS2 (BBS2 Produkte)
    Synonyme
    fb80a05 antikoerper, wu:fb80a05 antikoerper, DKFZp468B105 antikoerper, DKFZp469L0919 antikoerper, BBS antikoerper, 2410125H22Rik antikoerper, AI447581 antikoerper, Bardet-Biedl syndrome 2 antikoerper, bardet-biedl syndrome 2 antikoerper, Bardet-Biedl syndrome 2 (human) antikoerper, bbs2 antikoerper, BBS2 antikoerper, Bbs2 antikoerper
    Hintergrund
    This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, 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 forms a multiprotein BBSome complex with seven other BBS proteins.
    Molekulargewicht

    Observed_MW: 100 kDa

    Calculated_MW: 79 kDa

    Gen-ID
    583
    UniProt
    Q9BXC9
    Pathways
    Hedgehog Signalweg
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