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BBS2 antibody (AA 149-199)

The Rabbit Polyclonal anti-BBS2 antibody is suitable to detect BBS2 in samples from Human, Mouse and Rat. It has been validated for WB.
Catalog No. ABIN8119956
$385.00
Plus shipping costs $50.00
50 μL
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for BBS2 antibody (AA 149-199) (ABIN8119956)

Target

See all BBS2 Antibodies
BBS2 (Bardet-Biedl Syndrome 2 (BBS2))

Reactivity

  • 13
  • 6
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 11
  • 3
Rabbit

Clonality

  • 13
  • 1
Polyclonal

Conjugate

  • 14
This BBS2 antibody is un-conjugated

Application

  • 13
  • 5
  • 4
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

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

    Purpose

    BBS2 Antibody

    Specificity

    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.

    Immunogen

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

    Isotype

    IgG
  • Application Notes

    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.

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C/1 year

    Expiry Date

    12 months
  • Target

    BBS2 (Bardet-Biedl Syndrome 2 (BBS2))

    Alternative Name

    BBS2

    Background

    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

    Gene ID

    583

    UniProt

    Q9BXC9

    Pathways

    Hedgehog Signaling
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