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BBS2 anticorps (AA 149-199)

L’anticorps anti-BBS2 Polyclonal Lapin est utilisé pour la détection de BBS2 dans des échantillons de Humain, Souris et Rat. Il a été validé pour WB.
N° du produit ABIN8119956
450,00 €
Plus frais de livraison 40,00 € et TVA
50 μL
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour BBS2 anticorps (AA 149-199) (ABIN8119956)

Antigène

Voir toutes BBS2 Anticorps
BBS2 (Bardet-Biedl Syndrome 2 (BBS2))

Reactivité

  • 13
  • 6
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 11
  • 3
Lapin

Clonalité

  • 13
  • 1
Polyclonal

Conjugué

  • 14
Cet anticorp BBS2 est non-conjugé

Application

  • 13
  • 5
  • 4
  • 2
  • 1
Western Blotting (WB)
  • Épitope

    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 149-199

    Fonction

    BBS2 Antibody

    Specificité

    This antibody detects endogenous levels of BBS2 at Human/Mouse/Rat

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogène

    Synthesized peptide derived from human BBS2 AA range: 149-199

    Isotype

    IgG
  • Indications d'application

    WB 1:500-2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

    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/1 year

    Date de péremption

    12 months
  • Antigène

    BBS2 (Bardet-Biedl Syndrome 2 (BBS2))

    Autre désignation

    BBS2

    Sujet

    Background: 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.[provided by RefSeq, Oct 2014],

    Gene Name: BBS2

    Protein Name: BBS2

    ID gène

    583

    UniProt

    Q9BXC9

    Pathways

    Signalisation Hedgehog
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