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FMR1 Antikörper

Dieses 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

  • 77
  • 55
  • 44
  • 15
  • 6
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 63
  • 18
  • 2
Maus

Klonalität

  • 56
  • 27
Monoklonal

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

  • 69
  • 24
  • 22
  • 15
  • 14
  • 13
  • 12
  • 11
  • 8
  • 5
  • 4
  • 2
  • 1
  • 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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