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Cochlin (COCH) Peptide

COCH Reactivité: Mammifères Hôte: Synthetic BP, WB, IHC
N° du produit ABIN936639

Aperçu rapide pour Cochlin (COCH) Peptide (ABIN936639)

Antigène

COCH (Cochlin (COCH))

Origine

Mammifères

Source

  • 8
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Type de proteíne

    Synthetic

    Séquence

    AHPPTGKRLK KTPEKKTGNK DCKADIAFLI DGSFNIGQRR FNLQKNFVGK

    Attributs du produit

    A synthetic peptide for use as a blocking control in assays to test for specificity of COCH antibody,
    Alternative Names: COCH control peptide, COCH antibody Blocking Peptide, Anti-COCH Blocking Peptide, coagulation factor C homolog, cochlin, Limulus polyphemus Blocking Peptide, COCH-5B2 Blocking Peptide, COCH5B2 Blocking Peptide, DFNA9 Blocking Peptide
  • Indications d'application

    Optimal conditions should be determined by the investigator

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.

    Buffer

    PBS

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20 °C long term.
  • Antigène

    COCH (Cochlin (COCH))

    Sujet

    The protein encoded by this gene is highly conserved in human, mouse, and chicken, showing 94 % and 74 % 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.

    Poids moléculaire

    57 kDa
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