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GPR56 Antikörper (PE-Cy7)

Dieses Anti-GPR56-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von GPR56 in FACS. Geeignet für Human.
Produktnummer ABIN2659352

Kurzübersicht für GPR56 Antikörper (PE-Cy7) (ABIN2659352)

Target

Alle GPR56 Antikörper anzeigen
GPR56 (G Protein-Coupled Receptor 56 (GPR56))

Reaktivität

  • 43
  • 20
  • 5
  • 2
  • 2
Human

Wirt

  • 35
  • 8
Maus

Klonalität

  • 37
  • 6
Monoklonal

Konjugat

  • 25
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser GPR56 Antikörper ist konjugiert mit PE-Cy7

Applikation

  • 33
  • 19
  • 15
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
Flow Cytometry (FACS)

Klon

CG4
  • Aufreinigung

    The antibody was purified by affinity chromatography and conjugated with PE/Cy7 under optimal conditions. The solution is free of unconjugated PE/Cy7 and unconjugated antibody.

    Isotyp

    IgG1 kappa
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    Phosphate-buffered solution, pH 7.2, containing 0.09 % sodium azide and 0.2 % (w/v) BSA .

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handhabung

    Protect from prolonged exposure to light. Do not freeze.

    Lagerung

    4 °C

    Informationen zur Lagerung

    The antibody solution should be stored undiluted between 2°C and 8°C.
  • Target

    GPR56 (G Protein-Coupled Receptor 56 (GPR56))

    Andere Bezeichnung

    GPR56

    Hintergrund

    GPR56, also known as TM7XN1, is an orphan G-protein-coupled receptor (GPCR) containing seven transmembrane domains and a mucin-like domain in the N-terminal region. The total length of the human GPR56 gene is approximately 15 kb, and it consists of 13 exons and encodes 693 amino acids. GPR56 is expressed in a wide range of tissues, such as brain, thyroid gland, and heart. Mutations in human GPR56 gene were found to cause a specific brain malformation called bilateral frontoparietal polymicrogyria. Recently, GPR56 was found specifically expressed on cytotoxic NK and T lymphocytes, including CD8+, CD4+, and γδ T cells, which might affect the migratory properties of these cells. GPR56 was also found significantly downregulated in some cancer cells, suggesting that it may play a role in growth suppression and cancer metastasis.
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