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ube3a Antikörper (AA 1-860)

Dieses Anti-ube3a-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von ube3a in WB und FACS. Geeignet für Human und Affe.
Produktnummer ABIN7599564

Kurzübersicht für ube3a Antikörper (AA 1-860) (ABIN7599564)

Target

Alle ube3a Antikörper anzeigen
ube3a (Ubiquitin Protein Ligase E3A (ube3a))

Reaktivität

  • 57
  • 13
  • 9
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Affe

Wirt

  • 49
  • 8
Maus

Klonalität

  • 47
  • 10
Monoklonal

Konjugat

  • 31
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ube3a Antikörper ist unkonjugiert

Applikation

  • 33
  • 17
  • 17
  • 13
  • 13
  • 13
  • 9
  • 8
  • 8
  • 5
  • 3
  • 1
Western Blotting (WB), Flow Cytometry (FACS)

Klon

8I3
  • Bindungsspezifität

    • 15
    • 7
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-860

    Verwendungszweck

    Anti-UBE3A Picoband® Antibody (monoclonal, 8I3)

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    Anti-UBE3A Picoband® Antibody (monoclonal, 8I3) (ABIN7599564). Tested in Flow Cytometry, WB applications. This antibody reacts with Human, Monkey. 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 UBE3A recombinant protein (Position: M1-E860).

    Isotyp

    IgG2a
  • Applikationshinweise

    Western blot, 0.25-0.5 μg/mL, Human, Monkey
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    1. Abaied, L., Trabelsi, M., Chaabouni, M., Kharrat, M., Kraoua, L., M'rad, R., Tebib, N., Maazoul, F., Chaabouni, H. A novel UBE3A truncating mutation in large Tunisian Angelman syndrome pedigree. Am. J. Med. Genet. 152A: 141-146, 2010. 2. Albrecht, U., Sutcliffe, J. S., Cattanach, B. M., Beechey, C. V., Armstrong, D., Eichele, G., Beaudet, A. L. Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Nature Genet. 17: 75-78, 1997. 3. Camprubi, C., Guitart, M., Gabau, E., Coll, M. D., Villatoro, S., Oltra, S., Rosello, M., Ferrer, I., Monfort, S., Orellana, C., Martinez, F. Novel UBE3A mutations causing Angelman syndrome: different parental origin for single nucleotide changes and multiple nucleotide deletions or insertions. Am. J. Med. Genet. 149A: 343-348, 2009.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 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

    Store 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 freeze-thaw cycles.
  • Target

    ube3a (Ubiquitin Protein Ligase E3A (ube3a))

    Andere Bezeichnung

    UBE3A

    Hintergrund

    Synonyms: Extracellular calcium-sensing receptor, CaR

    Tissue Specificity: Expressed in the temporal lobe, frontal lobe, parietal lobe, hippocampus, and cerebellum. Also found in kidney, lung, liver, heart, skeletal muscle, placenta.

    Background: Ubiquitin-protein ligase E3A (UBE3A) also known as E6AP ubiquitin-protein ligase (E6AP) is an enzyme that in humans is encoded by the UBE3A gene. It is mapped to 15q11.2. This gene encodes an E3 ubiquitin-protein ligase, part of the ubiquitin protein degradation system. This imprinted gene is maternally expressed in brain and biallelically expressed in other tissues. Maternally inherited deletion of this gene causes Angelman Syndrome, characterized by severe motor and intellectual retardation, ataxia, hypotonia, epilepsy, absence of speech, and characteristic facies. The protein also interacts with the E6 protein of human papillomavirus types 16 and 18, resulting in ubiquitination and proteolysis of tumor protein p53. Alternative splicing of this gene results in three transcript variants encoding three isoforms with different N-termini. Additional transcript variants have been described, but their full length nature has not been determined.

    Molekulargewicht

    100 kDa

    Gen-ID

    7337

    UniProt

    Q05086

    Pathways

    Intracellular Steroid Hormone Receptor Signaling Pathway
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