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TTC8 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)

TTC8 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2734495
  • Target See all TTC8 Proteins
    TTC8 (Tetratricopeptide Repeat Domain 8 (TTC8))
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant 2
    Origin
    • 3
    • 1
    Human
    Source
    • 2
    • 2
    HEK-293 Cells
    Purification tag / Conjugate
    This TTC8 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human TTC8 / BBS8 (transcript variant 2) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product TTC8 Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Storage
    -80 °C
    Storage Comment
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target
    TTC8 (Tetratricopeptide Repeat Domain 8 (TTC8))
    Alternative Name
    Ttc8,bbs8 (TTC8 Products)
    Synonyms
    TTC8 Protein, bbs8 Protein, fk26c02 Protein, wu:fk26c02 Protein, zgc:136718 Protein, DKFZp459L2429 Protein, BBS8 Protein, RP51 Protein, 0610012F22Rik Protein, AV001447 Protein, tetratricopeptide repeat domain 8 Protein, TTC8 Protein, ttc8 Protein, lpa_01174 Protein, Ttc8 Protein
    Background
    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.
    Molecular Weight
    57.1 kDa
    NCBI Accession
    NP_938051
    Pathways
    Hedgehog Signaling
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