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TTC8 anticorps (N-Term)

Cet anticorps anti-TTC8 est un anticorps Lapin Polyclonal détectant TTC8 dans WB. Adapté pour Humain.
N° du produit ABIN1539117

Aperçu rapide pour TTC8 anticorps (N-Term) (ABIN1539117)

Antigène

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

Reactivité

  • 36
  • 19
  • 19
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 31
  • 4
  • 1
Lapin

Clonalité

  • 34
  • 2
Polyclonal

Conjugué

  • 16
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TTC8 est non-conjugé

Application

  • 36
  • 15
  • 15
  • 13
  • 13
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)

Clone

RB36550
  • Épitope

    • 16
    • 7
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 18-46, N-Term

    Purification

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

    Immunogène

    This TTC8 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 18-46 amino acids from the N-terminal region of human TTC8.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    TTC8 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Date de péremption

    6 months
  • Antigène

    TTC8 (Tetratricopeptide Repeat Domain 8 (TTC8))

    Autre désignation

    TTC8

    Sujet

    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.

    Poids moléculaire

    61534

    ID gène

    123016

    NCBI Accession

    NP_653197, NP_938051, NP_938052

    UniProt

    Q8TAM2

    Pathways

    Signalisation Hedgehog
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