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BBS2 anticorps (Middle Region)

BBS2 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN929334
  • Antigène Voir toutes BBS2 Anticorps
    BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
    Épitope
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Middle Region
    Reactivité
    • 10
    • 6
    • 4
    • 4
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Humain
    Hôte
    • 8
    • 3
    Lapin
    Clonalité
    • 10
    • 1
    Polyclonal
    Conjugué
    • 11
    Cet anticorp BBS2 est non-conjugé
    Application
    • 11
    • 4
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Purified
    Immunogène
    BBS2 antibody was raised in rabbit using the middle region of BBS2 as the immunogen
    Top Product
    Discover our top product BBS2 Anticorps primaire
  • Indications d'application
    WB: 0.2-1 µg/mL
    Optimal conditions should be determined by the investigator.
    Commentaires

    BBS2 Blocking Peptide, catalog no. 33R-7948, is also available for use as a blocking control in assays to test for specificity of this BBS2 antibody

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Concentration
    Lot specific
    Buffer
    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
    Conseil sur la manipulation
    Avoid repeated freeze/thaw cycles.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • Antigène
    BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
    Autre désignation
    BBS2 (BBS2 Produits)
    Synonymes
    anticorps fb80a05, anticorps wu:fb80a05, anticorps DKFZp468B105, anticorps DKFZp469L0919, anticorps BBS, anticorps 2410125H22Rik, anticorps AI447581, anticorps Bardet-Biedl syndrome 2, anticorps bardet-biedl syndrome 2, anticorps Bardet-Biedl syndrome 2 (human), anticorps bbs2, anticorps BBS2, anticorps Bbs2
    Sujet
    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
    Signalisation Hedgehog
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