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L1CAM Antikörper (Biotin)

Dieses Anti-L1CAM-Antikörper ist ein Kaninchen Monoklonal-Antikörper zur Detektion von L1CAM in FACS und ELISA. Geeignet für Human.
Produktnummer ABIN7608093

Kurzübersicht für L1CAM Antikörper (Biotin) (ABIN7608093)

Target

Alle L1CAM Antikörper anzeigen
L1CAM (L1 Cell Adhesion Molecule (L1CAM))

Reaktivität

  • 118
  • 39
  • 37
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 92
  • 35
  • 2
Kaninchen

Klonalität

  • 78
  • 50
  • 1
Monoklonal

Konjugat

  • 75
  • 12
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser L1CAM Antikörper ist konjugiert mit Biotin

Applikation

  • 72
  • 44
  • 43
  • 43
  • 26
  • 23
  • 18
  • 14
  • 13
  • 7
  • 7
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Flow Cytometry (FACS), ELISA

Klon

DM155
  • Verwendungszweck

    Biotinylated Anti-CD171 antibody(DM155), Rabbit mAb

    Aufreinigung

    Purified from cell culture supernatant by affinity chromatography

    Isotyp

    IgG
  • Applikationshinweise

    ELISA 1:5000-10000, Flow Cyt 1:100

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

    Lagerung

    -20 °C,-80 °C

    Informationen zur Lagerung

    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

    Haltbarkeit

    12 months
  • Target

    L1CAM (L1 Cell Adhesion Molecule (L1CAM))

    Andere Bezeichnung

    CD171

    Hintergrund

    The protein encoded by this gene is an axonal glycoprotein belonging to the immunoglobulin supergene family. The ectodomain, consisting of several immunoglobulin-like domains and fibronectin-like repeats (type III), is linked via a single transmembrane sequence to a conserved cytoplasmic domain. This cell adhesion molecule plays an important role in nervous system development, including neuronal migration and differentiation. Mutations in the gene cause X-linked neurological syndromes known as CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus). Alternative splicing of this gene results in multiple transcript variants, some of which include an alternate exon that is considered to be specific to neurons.

    UniProt

    P32004

    Pathways

    Synaptic Membrane
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