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FMR1 Antikörper

Dieses Anti-FMR1-Antikörper ist ein Kaninchen Monoklonal-Antikörper zur Detektion von FMR1 in WB und IHC. Geeignet für Human.
Produktnummer ABIN1679778

Kurzübersicht für FMR1 Antikörper (ABIN1679778)

Target

Alle FMR1 Antikörper anzeigen
FMR1 (Fragile X Mental Retardation 1 (FMR1))

Reaktivität

  • 79
  • 55
  • 43
  • 15
  • 6
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 61
  • 21
  • 2
Kaninchen

Klonalität

  • 54
  • 30
Monoklonal

Konjugat

  • 48
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser FMR1 Antikörper ist unkonjugiert

Applikation

  • 69
  • 25
  • 21
  • 15
  • 15
  • 14
  • 13
  • 9
  • 8
  • 8
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Kreuzreaktivität

    Human, Maus, Ratte

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human FMRP

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    FMR1 (Fragile X Mental Retardation 1 (FMR1))

    Andere Bezeichnung

    FMR1

    Hintergrund

    The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm. A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome. Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1). Multiple alternatively spliced transcript variants that encode different protein isoforms and which are located in different cellular locations have been described for this gene. [provided by RefSeq, May 2010],FMRP, FRAXA, POF, POF1,Cell Type Marker,Cell Type Marker_Dendrite marker,Cell Type Marker_Neuron marker,Cell Type Marker_Synapse marker,Epigenetics & Nuclear Signaling,Neurodegenerative Diseases,Neuroscience,RNA Binding,FMR1

    Molekulargewicht

    58 kDa/61 kDa/66 kDa/68 kDa/69 kDa/70 kDa/71 kDa

    Gen-ID

    2332

    UniProt

    Q06787

    Pathways

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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