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SPTA1 Antikörper (AA 356-475)

Der Maus Monoklonal Anti-SPTA1-Antikörper wurde für IHC (p) und WB validiert. Er ist geeignet, SPTA1 in Proben von Human zu detektieren.
Produktnummer ABIN6654217

Kurzübersicht für SPTA1 Antikörper (AA 356-475) (ABIN6654217)

Target

SPTA1 (Spectrin alpha Chain, Erythrocytic 1 (SPTA1))

Reaktivität

Human

Wirt

  • 2
  • 1
Maus

Klonalität

  • 3
Monoklonal

Konjugat

  • 3
Dieser SPTA1 Antikörper ist unkonjugiert

Applikation

Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)

Klon

SCNA-1R
  • Bindungsspezifität

    AA 356-475

    Aufreinigung

    Purified

    Reinheit

    Protein G affinity chromatography

    Immunogen

    A portion of amino acids 356-475 from the human protein was used as the immunogen for the recombinant SPTA1 antibody.

    Isotyp

    IgG1 kappa
  • Applikationshinweise

    The stated application concentrations are suggested starting points. Titration of the recombinant SPTA1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

    1. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.\. Western blot: 1-2 μg/mL,Immunohistochemistry (FFPE): 1-2 μg/mL for 30 min at RT,Prediluted IHC only format: incubate for 30 min at RT (1)

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    Konservierungsmittel

    Azide free

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Store the recombinant SPTA1 antibody at 2-8°C (with azide) or aliquot and store at -20°C or colder (without azide).
  • Target

    SPTA1 (Spectrin alpha Chain, Erythrocytic 1 (SPTA1))

    Andere Bezeichnung

    SPTA1 / Spectrin alpha 1

    Hintergrund

    This gene encodes a member of a family of molecular scaffold proteins that link the plasma membrane to the actin cytoskeleton and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. The encoded protein is primarily composed of 22 spectrin repeats which are involved in dimer formation. It forms a component of the erythrocyte plasma membrane. Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis-2, pyropoikilocytosis, and spherocytosis, type 3. [RefSeq]
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