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TTPA Antikörper (AA 13-278)

Dieses Anti-TTPA-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von TTPA in WB, ELISA und FACS. Geeignet für Human, Maus und Ratte.
Produktnummer ABIN7599931

Kurzübersicht für TTPA Antikörper (AA 13-278) (ABIN7599931)

Target

Alle TTPA Antikörper anzeigen
TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))

Reaktivität

  • 12
  • 5
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 14
  • 1
Kaninchen

Klonalität

  • 14
  • 1
Polyklonal

Konjugat

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser TTPA Antikörper ist unkonjugiert

Applikation

  • 14
  • 8
  • 4
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Bindungsspezifität

    • 7
    • 2
    • 2
    • 1
    • 1
    AA 13-278

    Verwendungszweck

    Anti-TTPA/TPP1 Antibody Picoband®

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    Anti-TTPA/TPP1 Antibody Picoband® (ABIN7599931). Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Aufreinigung

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human TTPA/TPP1 recombinant protein (Position: Q13-Q278).

    Isotyp

    IgG
  • Applikationshinweise

    Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Arita, M., Sato, Y., Miyata, A., Tanabe, T., Takahashi, E., Kayden, H. J., Arai, H., Inoue, K. Human alpha-tocopherol transfer protein: cDNA cloning, expression and chromosomal localization. Biochem. J. 306: 437-443, 1995. 2. Cavalier, L., Ouahchi, K., Kayden, H. J., Di Donato, S., Reutenauer, L., Mandel, J.-L., Koenig, M. Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families. Am. J. Hum. Genet. 62: 301-310, 1998. 3. Cellini, E., Piacentini, S., Nacmias, B., Forleo, P., Tedde, A., Bagnoli, S., Ciantelli, M., Sorbi, S. A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. Arch. Neurol. 59: 1952-1953, 2002.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Konzentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target

    TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))

    Andere Bezeichnung

    TTPA

    Hintergrund

    Synonyms: Interleukin-6, IL-6, Il6, Il-6

    Tissue Specificity: Expressed in activated macrophages (at protein level).

    Background: Alpha-tocopherol transfer protein is a protein that in humans is encoded by the TTPA gene. This gene encodes a soluble protein that binds alpha-trocopherol, a form of vitamin E, with high selectivity and affinity. This protein plays an important role in regulating vitamin E levels in the body by transporting vitamin E between membrane vesicles and facilitating the secretion of vitamin E from hepatocytes to circulating lipoproteins. Mutations in this gene cause hereditary vitamin E deficiency (ataxia with vitamin E deficiency, AVED) and retinitis pigmentosa.

    Molekulargewicht

    32 kDa, 37 kDa

    Gen-ID

    7274

    UniProt

    P49638
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