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TTC8 antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects TTC8 in WB and EIA. It exhibits reactivity toward Human.
Catalog No. ABIN955378

Quick Overview for TTC8 antibody (N-Term) (ABIN955378)

Target

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

Reactivity

  • 36
  • 19
  • 19
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 31
  • 4
  • 1
Rabbit

Clonality

  • 34
  • 2
Polyclonal

Conjugate

  • 16
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TTC8 antibody is un-conjugated

Application

  • 36
  • 15
  • 15
  • 13
  • 13
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 16
    • 8
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 17-46, N-Term

    Specificity

    This antibody detects TTC8 / BBS8 (N-term).

    Cross-Reactivity (Details)

    Species reactivity (tested):Human

    Purification

    Protein A column followed by peptide affinity purification

    Immunogen

    KLH conjugated synthetic peptide between 17-46 amino acids from the N-terminal region of human TTC8

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    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.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2 - 8 °C for up to six months or (in aliquots) at -20 °C for longer.
  • Target

    TTC8 (Tetratricopeptide Repeat Domain 8 (TTC8))

    Alternative Name

    TTC8 / BBS8

    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. Alternate transcriptional splice variants have been characterized.Synonyms: Bardet-Biedl syndrome 8 protein, TPR repeat protein 8, Tetratricopeptide repeat protein 8

    Gene ID

    123016

    NCBI Accession

    NP_653197

    Pathways

    Hedgehog Signaling
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