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BBS5 antibody (AA 224-317) (FITC)

The Rabbit Polyclonal anti-BBS5 antibody has been validated for . It is suitable to detect BBS5 in samples from Human.
Catalog No. ABIN7145244

Quick Overview for BBS5 antibody (AA 224-317) (FITC) (ABIN7145244)

Target

See all BBS5 Antibodies
BBS5 (Bardet-Biedl Syndrome 5 (BBS5))

Reactivity

  • 15
  • 7
  • 7
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 12
  • 6
Rabbit

Clonality

  • 14
  • 4
Polyclonal

Conjugate

  • 16
  • 1
  • 1
This BBS5 antibody is conjugated to FITC

Application

Please inquire
  • Binding Specificity

    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 224-317

    Cross-Reactivity

    Human

    Purification

    >95%, Protein G purified

    Immunogen

    Recombinant Human Bardet-Biedl syndrome 5 protein (224-317AA)

    Isotype

    IgG
  • Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Preservative: 0.03 % Proclin 300
    Constituents: 50 % Glycerol, 0.01M PBS, pH 7.4

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C,-80 °C

    Storage Comment

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target

    BBS5 (Bardet-Biedl Syndrome 5 (BBS5))

    Alternative Name

    BBS5

    Background

    Background: The BBSome complex is thought to function as a coat complex required for sorting of specific membrane proteins to the primary cilia. The BBSome complex is required for ciliogenesis but is dispensable for centriolar satellite function. This ciliogenic function is mediated in part by the Rab8 GDP/GTP exchange factor, which localizes to the basal body and contacts the BBSome. Rab8(GTP) enters the primary cilium and promotes extension of the ciliary membrane. Firstly the BBSome associates with the ciliary membrane and binds to RAB3IP/Rabin8, the guanosyl exchange factor (GEF) for Rab8 and then the Rab8-GTP localizes to the cilium and promotes docking and fusion of carrier vesicles to the base of the ciliary membrane. The BBSome complex, together with the LTZL1, controls SMO ciliary trafficking and contributes to the sonic hedgehog (SHH) pathway regulation. Required for BBSome complex ciliary localization but not for the proper complex assembly.

    Aliases: Bardet Biedl syndrome 5 protein antibody, Bardet-Biedl syndrome 5 protein antibody, BBS5 antibody, BBS5_HUMAN antibody

    UniProt

    Q8N3I7

    Pathways

    Hedgehog Signaling
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