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FMR1 Antikörper

Dieses Anti-FMR1-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von FMR1 in WB, IHC, ELISA, IF und IP. Geeignet für Human, Maus und Ratte.
Produktnummer ABIN5697696

Kurzübersicht für FMR1 Antikörper (ABIN5697696)

Target

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

Reaktivität

  • 77
  • 54
  • 43
  • 15
  • 6
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 62
  • 19
  • 2
Kaninchen

Klonalität

  • 55
  • 28
Polyklonal

Konjugat

  • 50
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser FMR1 Antikörper ist unkonjugiert

Applikation

  • 68
  • 24
  • 22
  • 15
  • 14
  • 13
  • 11
  • 10
  • 9
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)
  • Immunogen

    fragile X mental retardation 1

    Isotyp

    IgG
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Kommentare

    K-562 cells were subjected to SDS PAGE followed by western blot with FNab03172(FMR1 antibody) at dilution of 1:500

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    PBS with 0.02 % sodium azide and 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.

    Handhabung

    Avoid repeated freeze / thaw cycles.

    Lagerung

    -20 °C

    Haltbarkeit

    12 months
  • Target

    FMR1 (Fragile X Mental Retardation 1 (FMR1))

    Andere Bezeichnung

    FMR1

    Hintergrund

    Synonyms:FMRP Background: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.

    Gen-ID

    2332

    UniProt

    Q06787

    Pathways

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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