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FMR1 Antikörper

Der Maus Monoklonal Anti-FMR1-Antikörper wurde für WB validiert. Er ist geeignet, FMR1 in Proben von Human zu detektieren.
Produktnummer ABIN5002774

Kurzübersicht für FMR1 Antikörper (ABIN5002774)

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

  • 68
  • 25
  • 23
  • 15
  • 14
  • 13
  • 12
  • 11
  • 9
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)

Klon

8C2
  • Kreuzreaktivität

    Human

    Aufreinigung

    Mouse monoclonal antibody supplied in crude ascites with 0.09% (W/V) sodium azide.

    Immunogen

    This FMR1 antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 20-48 amino acids from human FMR1.

    Isotyp

    IgM
  • Applikationshinweise

    WB 1:300-5000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.5 μg/μL

    Buffer

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    Konservierungsmittel

    ProClin

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C for 12 months.

    Haltbarkeit

    12 months
  • Target

    FMR1 (Fragile X Mental Retardation 1 (FMR1))

    Andere Bezeichnung

    FMR1

    Hintergrund

    Synonyms: POF, FMRP, POF1, FRAXA, Synaptic functional regulator FMR1, Fragile X mental retardation protein 1, Protein FMR-1, FMR1

    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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