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TTC8 antibody (AA 271-533)

The Rabbit Polyclonal anti-TTC8 antibody (ABIN7873159) specifically detects TTC8 in WB, ELISA and FACS. The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7873159
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for TTC8 antibody (AA 271-533) (ABIN7873159)

Target

See all TTC8 Antibodies
TTC8 (Tetratricopeptide Repeat Domain 8 (TTC8))

Reactivity

  • 38
  • 19
  • 19
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 33
  • 4
  • 1
Rabbit

Clonality

  • 36
  • 2
Polyclonal

Conjugate

  • 18
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TTC8 antibody is un-conjugated

Application

  • 38
  • 15
  • 15
  • 13
  • 13
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 16
    • 8
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 271-533

    Purpose

    BBS8 Antibody / Bardet-Biedl syndrome 8 / TTC8

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids E271-Q533) was used as the immunogen for the BBS8 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the BBS8 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the BBS8 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    TTC8 (Tetratricopeptide Repeat Domain 8 (TTC8))

    Alternative Name

    BBS8

    Background

    Tetratricopeptide repeat domain 8 (TTC8) also known as Bardet-Biedl syndrome 8 (BBS8) is a protein that in humans is encoded by the TTC8 gene. This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is involved in the formation of cilia. A mutation in this gene has also been implicated in nonsyndromic retinitis pigmentosa. Alternative splicing results in multiple transcript variants.

    UniProt

    Q8TAM2

    Pathways

    Hedgehog Signaling
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