Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

KAL1 Antikörper (Center)

Dieses Anti-KAL1-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von KAL1 in WB und EIA. Geeignet für Human.
Produktnummer ABIN783480

Kurzübersicht für KAL1 Antikörper (Center) (ABIN783480)

Target

Alle KAL1 Antikörper anzeigen
KAL1 (Kallmann Syndrome 1 Sequence (KAL1))

Reaktivität

  • 30
  • 1
  • 1
Human

Wirt

  • 28
  • 2
Kaninchen

Klonalität

  • 29
  • 1
Polyklonal

Konjugat

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser KAL1 Antikörper ist unkonjugiert

Applikation

  • 23
  • 13
  • 13
  • 9
  • 3
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Bindungsspezifität

    • 15
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Center

    Spezifität

    This antibody detects Anosmin (Center).

    Kreuzreaktivität (Details)

    Species reactivity (tested):Human

    Aufreinigung

    Affinity chromatography

    Immunogen

    Raised against an 18 amino acid peptide near the center of human Anosmin
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    PBS containing 0.02 % sodium azide

    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 freezing and thawing.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    Store at 2 - 8 °C for up to one month or (in aliquots) at -20 °C for longer.
  • Target

    KAL1 (Kallmann Syndrome 1 Sequence (KAL1))

    Andere Bezeichnung

    Anosmin-1

    Hintergrund

    Mutations in Anosmin-1, an extracellular matrix-associated glycosylated protein, have been linked with Kallmann Syndrome (KS), an X-linked genetic disorder characterized by loss of smell caused by abnormal olfactory bulb development and delayed puberty caused by disrupted migration of the gonadotropin-releasing hormone neuron. Anosmin-1 has been shown to directly bind FGFR1 via its N-terminal cysteine-rich domain, whey-acidic protein-like domain, and its first FnIII repeat with the D2 and D3 ectodomains of FGFR1. It is thought that Anosmin-1 can modulate FGFR1 signaling and have opposing effects on the formation and activation of FGF2-FGFR1-heparing complex.Synonyms: ADMLX, Adhesion molecule-like X-linked, KAL, KAL1, KALIG1, Kallmann syndrome protein

    Gen-ID

    3730

    NCBI Accession

    NP_000207

    UniProt

    P23352
Sie sind hier:
Chat with us!