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TTC38 Antikörper (AA 267-469)

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch TTC38 in ELISA, WB, FACS und IF. Es zeigt Reaktivität gegenüber Proben von Human.
Produktnummer ABIN7873061
644,88 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für TTC38 Antikörper (AA 267-469) (ABIN7873061)

Target

Alle TTC38 Antikörper anzeigen
TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))

Reaktivität

  • 16
  • 9
Human

Wirt

  • 15
  • 1
Kaninchen

Klonalität

  • 16
Polyklonal

Konjugat

  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser TTC38 Antikörper ist unkonjugiert

Applikation

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

    • 6
    • 1
    • 1
    AA 267-469

    Verwendungszweck

    TTC38 Antibody / Tetratricopeptide repeat protein 38

    Aufreinigung

    Antigen affinity purified

    Immunogen

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

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the TTC38 antibody should be determined by the researcher.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    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.
  • Target

    TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))

    Andere Bezeichnung

    TTC38

    Hintergrund

    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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