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HGD Antikörper (AA 374-445)

Dieses Anti-HGD-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von HGD in WB, IHC und FACS. Geeignet für Human.
Produktnummer ABIN7601528

Kurzübersicht für HGD Antikörper (AA 374-445) (ABIN7601528)

Target

Alle HGD Antikörper anzeigen
HGD (Homogentisate 1,2-Dioxygenase (HGD))

Reaktivität

  • 40
  • 20
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 53
  • 5
Maus

Klonalität

  • 52
  • 6
Monoklonal

Konjugat

  • 29
  • 7
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser HGD Antikörper ist unkonjugiert

Applikation

  • 44
  • 21
  • 16
  • 13
  • 13
  • 13
  • 9
  • 6
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)

Klon

2F11E1
  • Bindungsspezifität

    • 15
    • 5
    • 5
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 374-445

    Verwendungszweck

    Anti-HGD Antibody Picoband® (monoclonal, 2F11E1)

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    Anti-HGD Antibody Picoband® (monoclonal, 2F11E1) (ABIN7601528). Tested in Flow Cytometry, IHC, WB applications. This antibody reacts with Human. 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 HGD recombinant protein (Position: D374-N445).

    Isotyp

    IgG2b
  • Applikationshinweise

    Western blot, 0.25-0.5 μg/mL, Human
    Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    1. Fernandez-Canon, J. M., Granadino, B., Beltran-Valero de Bernabe, D., Renedo, M., Fernandez-Ruiz, E., Penalva, M. A., Rodriguez de Cordoba, S. The molecular basis of alkaptonuria. Nature Genet. 14: 19-24, 1996. 2. Vilboux, T., Kayser, M., Introne, W., Suwannarat, P., Bernardini, I., Fischer, R., O'Brien, K., Kleta, R., Huizing, M., Gahl, W. A. Mutation spectrum of homogentisic acid oxidase (HGD) in alkaptonuria. Hum. Mutat. 30: 1611-1619, 2009.

    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 and 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

    HGD (Homogentisate 1,2-Dioxygenase (HGD))

    Andere Bezeichnung

    HGD

    Hintergrund

    Synonyms: Ras-related protein Rab-5A, RAB5A, RAB5

    Tissue Specificity: Widely expressed in fetal and adult tissues.

    Background: The HGD gene encodes homogentisate 1,2-dioxygenase (HGD), an enzyme involved in the catabolism of phenylalanine and tyrosine. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria. This gene is mapped to chromosome 3q21-q23 by a preliminary PCR screen of hamster/human somatic cell hybrid genomic DNA samples and by fluorescence in situ hybridization.

    Molekulargewicht

    50 kDa

    Gen-ID

    3081

    UniProt

    Q93099
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