Recombinant Rat CD30/TNFRSF8 Fc Chimera Protein, CF Summary
Product Specifications
Rat CD30 (Phe19-Leu255) Accession # EDL81069.1 | IEGRMDP | Mouse IgG2a (Glu98-Lys330) |
N-terminus | C-terminus | |
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.
11034-CD
Formulation | Lyophilized from a 0.2 μm filtered solution in PBS. |
Reconstitution | Reconstitute at 500 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 Mouse CD30 Ligand/TNFSF8 (732-CL) is immobilized at 0.250 μg/mL (100 μL/well), Recombinant Rat CD30/TNFRSF8 Mouse Fc Chimera Protein (Catalog # 11034-CD) binds with and ED50 of 20.0-120 ng/mL.
2 μg/lane of Recombinant Rat CD30/TNFRSF8 Mouse Fc Chimera Protein (Catalog # 11034-CD) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue staining, showing bands at 80-95 kDa and 160-190 kDa, respectively.
Reconstitution Calculator
Background: CD30/TNFRSF8
Lymphocyte activation antigen CD-30 (CD30), also known as Tumor necrosis factor receptor superfamily member 8 (TNFRSF8), is a type I transmembrane glycoprotein belonging to the TNFR superfamily (1, 2). Mature rat CD30 consists of an extracellular domain (ECD) containing four disulfide bonds and two cysteine-rich repeats, a transmembrane domain, and a cytoplasmic domain. Within the ECD, rat CD30 shares 45% and 79% amino acid (aa) sequence identity with human and mouse CD30, respectively. In human, isoforms of CD30 with truncated cytoplasmic domains can be generated as well as a soluble form, which is produced by proteolytic cleavage of CD30 at the cell surface and is found in serum (3, 4). CD30 is normally expressed on antigen-stimulated Th cells and B cells (5 ‑ 7). CD30 binds to CD30 Ligand/TNFSF8 which is expressed on activated Th cells, monocytes, granulocytes and medullary thymic epithelial cells (2, 6). Signaling via CD30‑CD30L has been shown to induce the activation and proliferation of T cells and the CD30–CD30L pathway has been implicated as a major player in secondary humoral immune responses (2). In the absence of antigenic stimulation, CD30 can still induce T cell expression of IL‑13 (8). CD30 contributes to thymic negative selection by inducing the apoptotic cell death of CD4+CD8+ T cells (8, 9). In B cells, CD30 ligation promotes cellular proliferation and antibody production in addition to the expression of CXCR4, CCL3, and CCL5 (6, 10). Soluble CD30 retains the ability to bind CD30 Ligand and functions as an inhibitor of normal CD30 signaling (11). CD30 is up‑regulated in Hodgkin's disease (on Reed-Sternberg cells), other lymphomas, chronic inflammation, and autoimmunity (12).
- Hehlgans, T. & Pfeffer, K. (2005) Immunology 115(1):1–20.
- Kennedy, M.K. et al. (2006) Immunology 118:143.
- van der Weyden, C.A. et al. (2017). Blood Cancer J. 7:e603
- Buchan, S.L. and Al-Shamkhani, A. (2012) PLoS ONE 7:e45244.
- Hamann, D. et al. (1996) J. Immunol. 156:1387.
- Shanebeck, S.D. et al. (1995) Eur. J. Immunol. 25:2147.
- Gruss, H.-J. et al. (1994) Blood 83:2045.
- Harlin, H. et al. (2002) J. Immunol. 169:2451.
- Amakawa, R. et al. (1996) Cell 84:551.
- Vinante, F. et al. (2002) Blood 99:52.
- Hargreaves, P.G. and A. Al-Shamkhani (2002) Eur. J. Immunol. 32:163.
- Oflzoglu E. et al. (2009) Adv. Exp. Med. Biol. 647:174.
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