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TTC38 anticorps (AA 267-469)

Cet anticorps Lapin Polyclonal détecte spécifiquement TTC38 dans ELISA, WB, FACS et IF. Il présente une réactivité avec des échantillons de Humain.
N° du produit ABIN7873061
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour TTC38 anticorps (AA 267-469) (ABIN7873061)

Antigène

Voir toutes TTC38 Anticorps
TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))

Reactivité

  • 16
  • 9
Humain

Hôte

  • 15
  • 1
Lapin

Clonalité

  • 16
Polyclonal

Conjugué

  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TTC38 est non-conjugé

Application

  • 7
  • 5
  • 3
  • 1
  • 1
  • 1
ELISA, Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (IF)
  • Épitope

    • 6
    • 1
    • 1
    AA 267-469

    Fonction

    TTC38 Antibody / Tetratricopeptide repeat protein 38

    Purification

    Antigen affinity purified

    Immunogène

    E. coli-derived recombinant human protein (amino acids E267-Q469) was used as the immunogen for the TTC38 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the TTC38 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 TTC38 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

    TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))

    Autre désignation

    TTC38

    Sujet

    TTC38 (tetratricopeptide repeat domain 38) is a 469 amino acid protein that contains three TPR repeats and belongs to the TTC38 family. The gene that encodes TTC38 consists of over 26,000 bases and maps to 22q13. Housing over 500 genes, chromosome 22 is the second smallest chromosome in the human genome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. In addition, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.

    UniProt

    Q5R3I4
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