Recombinant Cynomolgus CD48/SLAMF2 His-tag Protein, CF
Recombinant Cynomolgus CD48/SLAMF2 His-tag Protein, CF Summary
Product Specifications
Gln27-Ser217, 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.
10399-CD
Formulation | Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. |
Reconstitution | Reconstitute at 200 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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Scientific Data
When Recombinant Human 2B4/CD244/SLAMF4 Fc Chimera (Catalog # 1039-2B) is immobilized at 0.5 µg/mL, 100 µL/well, the concentration of Recombinant Cynomolgus Monkey CD48/SLAMF2 His-tag (Catalog # 10399-CD) that produces 50% of the optimal binding response is approximately 75-450 ng/mL.
2 μg/lane of Recombinant Cynomolgus Monkey CD48/SLAMF2 His-tag (Catalog # 10399-CD) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue staining, showing bands at 39-44 kDa.
Reconstitution Calculator
Background: CD48/SLAMF2
CD48, also known as BLAST-1, BCM-1, and SLAMF2, is a 65 kDa GPI-linked protein in the CD2 family of immunoglobulin superfamily molecules (1-3). The cynomolgus CD48 cDNA encodes a 241 amino acid (aa) precursor that includes a 26 aa signal sequence, a 191 aa mature protein that contains one Ig-like V-type domain and one Ig-like C2-type domain, and a 23 aa C-terminal propeptide (4). A soluble form of CD48 has been detected in the serum of lymphoid leukemia and arthritis patients (5). Cynomolgus CD48 shares approximately 90% aa sequence identity with human CD48. CD48 is expressed on most lineage-committed hematopoietic cells but not on hematopoietic stem cells or multipotent hematopoietic progenitors (4, 6). Among dendritic cells (DC), CD48 is selectively expressed on circulating myeloid DC and resident bone marrow and thymus DC (7). CD2, 2B4, and heparin sulfate function as CD48 ligands (8‑10). CD48 is competent to transduce signals and can also trigger signaling through CD2 or 2B4 (8, 11). CD48-CD2 interactions promote T cell activation and class switching to IgG2a in B cells (8, 12). High affinity CD48‑2B4 interactions can either promote or inhibit NK cell and cytotoxic T cell (CTL) activation (7, 11, 13, 14). In mouse, CD48-2B4 ligation does not directly trigger CTL activity but enhances signaling from the T cell receptor (13). CD48-2B4 mediated inhibition of NK cell activity is distinct from MHC I‑restricted mechanisms (15). CD48 expressed on NK cells is co-activating, whereas CD48 expressed on other cell types inhibits NK cell activation (14). Both CD48 expressing and non‑expressing cells can be targets of NK cell or CTL-mediated lysis (13, 16).
- Assarsson, E. et al. (2005) J. Immunol. 175:2045.
- Bhat, R. et al. (2006) J. Leukocyte Biol. 79:417.
- Loertscher, R. and P. Lavery (2002) Transpl. Immunol. 9:93.
- Wong, Y.W. et al. (1990) J. Exp. Med. 171:2115.
- Smith, G.M. et al. (1997) J. Clin. Immunol. 17:502.
- Keil, M.J. et al. (2005) Cell 121:1109.
- Morandi, B. et al. (2005) J. Immunol. 175:3690.
- Kato, K. et al. (1992) J. Exp. Med. 176:1241.
- Latchman, Y. et al. (1998) J. Immunol. 161:5809.
- Ianelli, C.J. et al. (1998) J. Biol. Chem. 273:23367.
- Messmer, B. et al. (2006) J. Immunol. 176:4646.
- Gao, N. et al. (2005) J. Immunol. 174:4113.
- Lee, K-M. et al. (2003) J. Immunol. 170:4881.
- Lee, K-M. et al. (2006) Blood 107:3181.
- McNerney, M.E. et al. (2005) Blood 106:1337.
- Lee, K-M. et al. (2004) J. Exp. Med. 199:1245.
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