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Ataxin 1 Antikörper

Dieser Anti-Ataxin 1 Antikörper ist ein Maus Monoklonal Antikörper zur Detektion von Ataxin 1 in WB, IHC, ELISA, IF und FACS. Geeignet für Human.
Produktnummer ABIN865485

Kurzübersicht für Ataxin 1 Antikörper (ABIN865485)

Target

Alle Ataxin 1 (ATXN1) Antikörper anzeigen
Ataxin 1 (ATXN1)

Reaktivität

  • 85
  • 59
  • 36
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 71
  • 48
  • 1
Maus

Klonalität

  • 62
  • 58
Monoklonal

Konjugat

  • 42
  • 9
  • 7
  • 7
  • 5
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Ataxin 1 Antikörper ist unkonjugiert

Applikation

  • 90
  • 41
  • 40
  • 33
  • 33
  • 31
  • 23
  • 23
  • 7
  • 7
  • 6
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)

Klon

2F5
  • Aufreinigung

    Ascitic fluid

    Immunogen

    Purified recombinant fragment of human ATXN1 expressed in E. Coli.

    Isotyp

    IgG1
  • Applikationshinweise

    WB: 1/500 - 1/2000, IHC: 1/200 - 1/1000, IF: 1/200 - 1/1000, FC: 1/200-1/400 ELISA: Propose dilution 1/10000. Figure 3: Immunofluorescence

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    100g/100l

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    4 °C
  • Target

    Ataxin 1 (ATXN1)

    Andere Bezeichnung

    ATXN1

    Hintergrund

    The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. Synonyms: ATX1, SCA1, D6S504E, ATXN1

    Molekulargewicht

    87kDa

    Gen-ID

    6310

    Pathways

    Synaptic Membrane
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