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BBS10 antibody (C-Term)

The Rabbit Polyclonal anti-BBS10 antibody has been validated for WB and FACS. It is suitable to detect BBS10 in samples from Human.
Catalog No. ABIN651074

Quick Overview for BBS10 antibody (C-Term) (ABIN651074)

Target

See all BBS10 Antibodies
BBS10 (Bardet-Biedl Syndrome 10 (BBS10))

Reactivity

  • 41
  • 2
  • 1
  • 1
Human

Host

  • 40
  • 1
Rabbit

Clonality

  • 41
Polyclonal

Conjugate

  • 13
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This BBS10 antibody is un-conjugated

Application

  • 31
  • 15
  • 13
  • 13
  • 8
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), Flow Cytometry (FACS)

Clone

RB24715
  • Binding Specificity

    • 15
    • 7
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 515-544, C-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This BBS10 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 515-544 amino acids from the C-terminal region of human BBS10.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. FC: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    BBS10 (Bardet-Biedl Syndrome 10 (BBS10))

    Alternative Name

    BBS10

    Background

    BBS10 is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by progressive retinal degeneration, 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 is likely not a ciliary protein but rather has distant sequence homology to type II chaperonins. As a molecular chaperone, this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes.

    Molecular Weight

    80838

    Gene ID

    79738

    NCBI Accession

    NP_078961

    UniProt

    Q8TAM1
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