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BBS2 antibody (Middle Region)

BBS2 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN929334
  • Target See all BBS2 Antibodies
    BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
    Binding Specificity
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Middle Region
    Reactivity
    • 10
    • 6
    • 4
    • 4
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Human
    Host
    • 8
    • 3
    Rabbit
    Clonality
    • 10
    • 1
    Polyclonal
    Conjugate
    • 11
    This BBS2 antibody is un-conjugated
    Application
    • 11
    • 4
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Purified
    Immunogen
    BBS2 antibody was raised in rabbit using the middle region of BBS2 as the immunogen
    Top Product
    Discover our top product BBS2 Primary Antibody
  • Application Notes
    WB: 0.2-1 µg/mL
    Optimal conditions should be determined by the investigator.
    Comment

    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.
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • Target
    BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
    Alternative Name
    BBS2 (BBS2 Products)
    Synonyms
    fb80a05 antibody, wu:fb80a05 antibody, DKFZp468B105 antibody, DKFZp469L0919 antibody, BBS antibody, 2410125H22Rik antibody, AI447581 antibody, Bardet-Biedl syndrome 2 antibody, bardet-biedl syndrome 2 antibody, Bardet-Biedl syndrome 2 (human) antibody, bbs2 antibody, BBS2 antibody, Bbs2 antibody
    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 six other BBS proteins. Synonyms: Polyclonal BBS2 antibody, Anti-BBS2 antibody, Bardet-Biedl syndrome 2 antibody, BBS antibody, MGC20703 antibody.
    Pathways
    Hedgehog Signaling
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