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BBS2 Antikörper (N-Term)

BBS2 Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN929335
  • Target Alle BBS2 Antikörper anzeigen
    BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
    Bindungsspezifität
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    N-Term
    Reaktivität
    • 10
    • 6
    • 4
    • 4
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Human
    Wirt
    • 8
    • 3
    Kaninchen
    Klonalität
    • 10
    • 1
    Polyklonal
    Konjugat
    • 11
    Dieser BBS2 Antikörper ist unkonjugiert
    Applikation
    • 11
    • 4
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Aufreinigung
    Purified
    Immunogen
    BBS2 antibody was raised in rabbit using the N terminal of BBS2 as the immunogen
    Top Product
    Discover our top product BBS2 Primärantikörper
  • Applikationshinweise
    Optimal conditions should be determined by the investigator.
    Kommentare

    BBS2 Blocking Peptide, catalog no. 33R-3554, is also available for use as a blocking control in assays to test for specificity of this BBS2 antibody

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Konzentration
    Lot specific
    Buffer
    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
    Handhabung
    Avoid repeated freeze/thaw cycles.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • 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 six other BBS proteins. Synonyms: Polyclonal BBS2 antibody, Anti-BBS2 antibody, Bardet-Biedl syndrome 2 antibody, BBS antibody, MGC20703 antibody.
    Pathways
    Hedgehog Signalweg
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