Mouse LRRC32/GARP Antibody Summary
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of Mouse LRRC32/GARP by Western Blot. Western blot shows lysates of mouse spleen non-B cells. PVDF Membrane was probed with 0.1 µg/mL of Sheep Anti-Mouse LRRC32/GARP Antigen Affinity-purified Polyclonal Antibody (Catalog # AF6229) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # HAF016). A specific band was detected for LRRC32/GARP at approximately 85 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
LRRC32/GARP in bEnd.3 Mouse Cell Line. LRRC32/GARP was detected in immersion fixed bEnd.3 mouse endothelioma cell line using Sheep Anti-Mouse LRRC32/ GARP Antigen Affinity-purified Polyclonal Antibody (Catalog # AF6229) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the Northern-Lights™ 557-conjugated Anti-Sheep IgG Secondary Antibody (red; Catalog # NL010) and counterstained with DAPI (blue). Specific staining was localized to cytoplasm. View our protocol for Fluorescent ICC Staining of Cells on Coverslips.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 degreesC as supplied. 1 month, 2 to 8 degreesC under sterile conditions after reconstitution. 6 months, -20 to -70 degreesC under sterile conditions after reconstitution.
Background: LRRC32/GARP
Leucine-rich repeat protein 32 (LRRC32), also known as GARP (glycoprotein A repetitions predominant), is an 80 kDa type I transmembrane glycoprotein (1). Mature mouse LRRC32 consists of a 608 amino acid (aa) extracellular domain (ECD) that contains 22 leucine-rich repeats, a 21 aa transmembrane segment, and a 14 aa cytoplasmic domain (2-4). Within the ECD, mouse LRRC32 shares 80 and 94% aa sequence identity with human and rat LRRC32, respectively. LRRC32 is widely expressed during embryogenesis and on adult platelets (4, 5). Among T cells, it is selectively expressed on activated FOXP3+ regulatory T cells (Treg) (6-10). LRRC32 expression promotes the acquisition of a Treg phenotype including reduced cellular proliferation, reduced cytokine secretion, and the capacity to suppress the proliferation of naïve T cells (6-8). LRRC32 binds directly to the TGF-beta latency associated peptide (LAP) and tethers latent TGF-beta on the surface of activated Treg cells (9, 10). The presentation of TGF-beta on Tregs contributes to their ability to suppress naïve T cell proliferation (11).
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- Bella, J. et al. (2008) Cell Mol Life Sci. 65:2307.
- Roubin, R. et al. (1996) Int. J. Dev. Biol. 40:545.
- Macaulay, I.C. et al. (2007) Blood 109:3260.
- Wang, R. et al. (2008) PloS ONE 3:e2705.
- Wang, R. et al. (2009) Proc. Natl. Acad. Sci. 106:13439.
- Probst-Kepper, M. et al. (2009) J. Cell. Mol. Med. 13:3343.
- Tran, D.Q. et al. (2009) Proc. Natl. Acad. Sci. 106:13445.
- Stockis, J. et al. (2009) Eur. J. Immunol. 39:3315.
- Vignali, D.A. et al. (2008) Nat. Rev. Immunol. 8:523.
Product Datasheets
Citation for Mouse LRRC32/GARP Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
1 Citation: Showing 1 - 1
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B lymphocytes confer immune tolerance via cell surface GARP-TGF-? complex
Authors: CH Wallace, BX Wu, M Salem, EA Ansa-Addo, A Metelli, S Sun, G Gilkeson, MJ Shlomchik, B Liu, Z Li
JCI Insight, 2018-04-05;3(7):.
Species: Mouse
Sample Types: Cell Lysates
Applications: Western Blot
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