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

PCDH15 Antikörper

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch PCDH15 in WB und ELISA. Er zeigt eine Reaktivität gegenüber Human, Maus und Ratte.
Produktnummer ABIN2463319

Kurzübersicht für PCDH15 Antikörper (ABIN2463319)

Target

Alle PCDH15 Antikörper anzeigen
PCDH15 (Protocadherin-15 (PCDH15))

Reaktivität

  • 16
  • 8
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 13
  • 3
  • 3
Kaninchen

Klonalität

  • 16
  • 3
Polyklonal

Konjugat

  • 19
Dieser PCDH15 Antikörper ist unkonjugiert

Applikation

  • 16
  • 10
  • 6
  • 5
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Aufreinigung

    Antibody is purified by peptide affinity chromatography method.

    Immunogen

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human PCDH15.
  • Applikationshinweise

    PCDH15 antibody can be used for detection of PCDH15 by ELISA at 1:62500. PCDH15 antibody can be used for detection of PCDH15 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    Konzentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Handhabung

    As with any antibody avoid repeat freeze-thaw cycles.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store PCDH15 antibody at -20 °C.
  • Target

    PCDH15 (Protocadherin-15 (PCDH15))

    Andere Bezeichnung

    PCDH15

    Hintergrund

    PCDH15 is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. PCDH15 consists of a signal peptide, 11 extracellular calcium-binding domains, a transmembrane domain and a unique cytoplasmic domain. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene have been associated with hearing loss, which is consistent with its location at the Usher syndrome type 1F (USH1F) critical region on chromosome 10.

    Molekulargewicht

    80 kDa

    Gen-ID

    65217

    UniProt

    A2A3E5

    Pathways

    Sensory Perception of Sound
Sie sind hier:
Chat with us!