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COCH Antikörper

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch COCH in ELISA. Er zeigt eine Reaktivität gegenüber Human, Maus und Ratte.
Produktnummer ABIN5703508

Kurzübersicht für COCH Antikörper (ABIN5703508)

Target

Alle COCH Antikörper anzeigen
COCH (Cochlin (COCH))

Reaktivität

  • 39
  • 12
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 37
  • 2
Kaninchen

Klonalität

  • 39
Polyklonal

Konjugat

  • 21
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser COCH Antikörper ist unkonjugiert

Applikation

  • 29
  • 17
  • 12
  • 10
  • 3
  • 2
  • 2
ELISA
  • Immunogen

    coagulation factor C homolog, cochlin (Limulus polyphemus)

    Isotyp

    IgG
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol  pH 7.3

    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 freeze / thaw cycles.

    Lagerung

    -20 °C

    Haltbarkeit

    12 months
  • Target

    COCH (Cochlin (COCH))

    Andere Bezeichnung

    COCH

    Hintergrund

    Synonyms:COCH5B2 Background:The protein encoded by this gene is highly conserved in human, mouse, and chicken, showing 94 % and 79 % amino acid identity of human to mouse and chicken sequences, respectively. Hybridization to this gene was detected in spindle-shaped cells located along nerve fibers between the auditory ganglion and sensory epithelium. These cells accompany neurites at the habenula perforata, the opening through which neurites extend to innervate hair cells. This and the pattern of expression of this gene in chicken inner ear paralleled the histologic findings of acidophilic deposits, consistent with mucopolysaccharide ground substance, in temporal bones from DFNA9 (autosomal dominant nonsyndromic sensorineural deafness 9) patients. Mutations that cause DFNA9 have been reported in this gene. Alternative splicing results in multiple transcript variants encoding the same protein. Additional splice variants encoding distinct isoforms have been described but their biological validities have not been demonstrated.

    Gen-ID

    1690

    UniProt

    O43405

    Pathways

    Sensory Perception of Sound
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