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FMR1 Antikörper

Dieser Maus Monoklonal Antikörper erkennt spezifisch FMR1 in IHC, ELISA und ICC. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN969148

Kurzübersicht für FMR1 Antikörper (ABIN969148)

Target

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

Reaktivität

  • 94
  • 73
  • 61
  • 15
  • 6
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 78
  • 19
  • 2
Maus

Klonalität

  • 53
  • 46
Monoklonal

Konjugat

  • 45
  • 6
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser FMR1 Antikörper ist unkonjugiert

Applikation

  • 85
  • 36
  • 33
  • 24
  • 15
  • 15
  • 14
  • 13
  • 8
  • 8
  • 4
  • 2
  • 1
  • 1
Immunohistochemistry (IHC), ELISA, Immunocytochemistry (ICC)

Klon

4G9
  • Verwendungszweck

    FMR1 Antibody

    Aufreinigung

    Ascitic fluid

    Immunogen

    Purified recombinant fragment of human FMR1 expressed in E. Coli.

    Isotyp

    IgG1
  • Applikationshinweise

    ELISA: 1/10000

    ICC: 1/200 - 1/1000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Ascitic fluid containing 0.03 % sodium azide.

    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,-20 °C

    Informationen zur Lagerung

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    FMR1 (Fragile X Mental Retardation 1 (FMR1))

    Andere Bezeichnung

    FMR1

    Hintergrund

    FMR1, also known as POF, FMRP, FRAXA. Entrez Protein: NP_002015. It is an RNA-binding protein that associates with polyribosomes and is a likely component of a messenger ribonuclear protein (mRNP) particle The 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). RNA-binding protein that plays a role in intracellular RNA transport and in the regulation of translation of target mRNAs.

    Molekulargewicht

    71 kDa

    Gen-ID

    2332

    UniProt

    Q06787

    Pathways

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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