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TTC8 anticorps (AA 271-533)

Cet anticorps anti-TTC8 Polyclonal Lapin (ABIN7873159) détecte spécifiquement TTC8 dans WB, ELISA et FACS. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.
N° du produit ABIN7873159
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour TTC8 anticorps (AA 271-533) (ABIN7873159)

Antigène

Voir toutes TTC8 Anticorps
TTC8 (Tetratricopeptide Repeat Domain 8 (TTC8))

Reactivité

  • 38
  • 19
  • 19
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 33
  • 4
  • 1
Lapin

Clonalité

  • 36
  • 2
Polyclonal

Conjugué

  • 18
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TTC8 est non-conjugé

Application

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

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

    Fonction

    BBS8 Antibody / Bardet-Biedl syndrome 8 / TTC8

    Purification

    Antigen affinity purified

    Immunogène

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

    Isotype

    IgG
  • Indications d'application

    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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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.
  • Antigène

    TTC8 (Tetratricopeptide Repeat Domain 8 (TTC8))

    Autre désignation

    BBS8

    Sujet

    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

    Signalisation Hedgehog
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