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BBS2 anticorps

BBS2 Reactivité: Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7263435
  • Antigène Voir toutes BBS2 Anticorps
    BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
    Reactivité
    • 11
    • 5
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Souris, Rat
    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)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human BBS2 (NP_114091.3).
    Isotype
    IgG
    Top Product
    Discover our top product BBS2 Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • 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 seven other BBS proteins.
    Poids moléculaire

    Observed_MW: 100 kDa

    Calculated_MW: 79 kDa

    ID gène
    583
    UniProt
    Q9BXC9
    Pathways
    Signalisation Hedgehog
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