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LRRC32 antibody (PE)

This anti-LRRC32 antibody is a Rat Monoclonal antibody detecting LRRC32 in FACS and IHC. Suitable for Mouse.
Catalog No. ABIN2662727

Quick Overview for LRRC32 antibody (PE) (ABIN2662727)

Target

See all LRRC32 Antibodies
LRRC32 (Leucine Rich Repeat Containing 32 (LRRC32))

Reactivity

  • 27
  • 10
  • 9
  • 1
Mouse

Host

  • 25
  • 11
  • 1
  • 1
Rat

Clonality

  • 26
  • 12
Monoclonal

Conjugate

  • 24
  • 6
  • 3
  • 2
  • 2
  • 1
This LRRC32 antibody is conjugated to PE

Application

  • 20
  • 17
  • 16
  • 9
  • 4
  • 4
  • 2
  • 1
  • 1
Flow Cytometry (FACS), Immunohistochemistry (IHC)

Clone

F011-5
  • Purification

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

    Isotype

    IgG2a kappa
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Concentration

    0.2 mg/mL

    Buffer

    Phosphate-buffered solution, pH 7.2, containing 0.09 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

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

    Handling Advice

    Protect from prolonged exposure to light. Do not freeze.

    Storage

    4 °C

    Storage Comment

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

    LRRC32 (Leucine Rich Repeat Containing 32 (LRRC32))

    Alternative Name

    GARP

    Background

    Glycoprotein A Repetitions Predominant (GARP), also known as leucine rich repeat containing protein 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. It 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. 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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