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LRRC32 Antikörper (APC)

Dieses Anti-LRRC32-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von LRRC32 in BCA. Geeignet für Human.
Produktnummer ABIN2658317

Kurzübersicht für LRRC32 Antikörper (APC) (ABIN2658317)

Target

Alle LRRC32 Antikörper anzeigen
LRRC32 (Leucine Rich Repeat Containing 32 (LRRC32))

Reaktivität

  • 29
  • 12
  • 10
  • 1
Human

Wirt

  • 25
  • 13
  • 4
  • 1
Maus

Klonalität

  • 26
  • 17
Monoklonal

Konjugat

  • 26
  • 6
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Dieser LRRC32 Antikörper ist konjugiert mit APC

Applikation

  • 21
  • 20
  • 17
  • 13
  • 5
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Biochemical Assay (BCA)

Klon

7B11
  • Aufreinigung

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

    Isotyp

    IgG2b 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

    LRRC32 (Leucine Rich Repeat Containing 32 (LRRC32))

    Andere Bezeichnung

    GARP

    Hintergrund

    Glycoprotein A Repetitions Predominant (GARP), also known as leucine rich repeat containing 32 (LRC32), is a 80 kD type I membrane glycoprotein with 20 leucine rich repeats in the extracellular portion of the protein. GARP was found on the surface of megakaryocytes, platelets, and activated Tregs (CD4+, CD25+, FoxP3+ cells) and serves as a receptor for latent TGF-β. Recent evidence suggests that GARP may play a role in controlling suppressor function of Tregs. A mutation in GARP has been reported in a large Samaritan kindred with Usher syndrome type 1, an autosomal recessive disease characterized by profound congenital sensorineural deafness, vestibular dysfunction, and progressive visual loss. In addition, it has been found that GARP mRNA is highly amplified in different tumors, which indicates that tumor cells may use GARP to express TGF-β or to capture TGF-β from their surroundings, resulting in local suppression of anti-tumor immune responses or the induction of Tregs.

    Pathways

    Activated T Cell Proliferation
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