Recombinant Mouse LRRC32/GARP Protein, CF Summary
Product Specifications
Ile18-Asn628, with a C-terminal 6-His tag
Analysis
Product Datasheets
Carrier Free
CF stands for Carrier Free (CF). We typically add Bovine Serum Albumin (BSA) as a carrier protein to our recombinant proteins. Adding a carrier protein enhances protein stability, increases shelf-life, and allows the recombinant protein to be stored at a more dilute concentration. The carrier free version does not contain BSA.
In general, we advise purchasing the recombinant protein with BSA for use in cell or tissue culture, or as an ELISA standard. In contrast, the carrier free protein is recommended for applications, in which the presence of BSA could interfere.
6229-LR
Formulation | Lyophilized from a 0.2 μm filtered solution in HEPES, NaCl, PEG 3350 and CHAPS. |
Reconstitution | Reconstitute at 300 μg/mL in PBS. |
Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
Stability & Storage: | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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Reconstitution Calculator
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).
- Battaglia, M. and M.G. Roncarolo (2009) Eur. J. Immunol. 39:3296.
- Ollendorff, V. et al. (1994) Cell Growth Differ. 5:213.
- 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.
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