Recombinant Mouse CD74 Protein, CF Summary
Details of Functionality |
Measured by the ability of the immobilized protein to support the adhesion of HeLa human cervical epithelial carcinoma cells. When 5 x 104 cells per well are added to Recombinant Mouse CD74 coated plates, cell adhesion is enhanced in a dose dependent manner. The ED50 for this effect is 0.3-1.5 μg/mL. Optimal dilutions should be determined by each laboratory for each application. |
Source |
Chinese Hamster Ovary cell line, CHO-derived mouse CD74 protein Gln56-Leu215, with an N-terminal HA-tag (YPYDVPDYA) |
Accession # |
|
N-terminal Sequence |
Tyr |
Protein/Peptide Type |
Recombinant Proteins |
Gene |
Cd74 |
Purity |
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
19.4 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
SDS-PAGE |
26-40 kDa, reducing conditions |
Packaging, Storage & Formulations
Storage |
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 3 months, -20 to -70 °C under sterile conditions after reconstitution.
|
Buffer |
Lyophilized from a 0.2 μm filtered solution in PBS. |
Purity |
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain |
Reconstitution Instructions |
Reconstitute at 100 μg/mL in PBS. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Mouse CD74 Protein, CF
Background
CD74, also known as Invariant chain (Ii) and p33, is a type 2 transmembrane glycoprotein that plays an important role in adaptive immunity, inflammation, and cancer (1). Mature mouse CD74 consists of a 29 amino acid (aa) cytoplasmic domain, a 29 aa transmembrane segment, and a 224 aa extracellular domain (ECD) that contains one thyroglobulin type 1 domain (2). Alternate splicing generates a short isoform that lacks the thyroglobulin domain (2). Within the ECD, mouse CD74 shares 75% and 88% aa sequence identity with human and rat CD74, respectively. CD74 functions as a chaperone for MHC class II molecules on antigen presenting cells and undergoes progressive proteolysis during class II trafficking and antigenic peptide loading (3). Full length CD74 assembles into trimers which then associate with class II molecules in nonameric complexes on the cell surface (4, 5). CD74 also associates with CD44 and binds with high affinity to the cytokine MIF, leading to inflammatory leukocyte responses, protection from tissue fibrosis, B cell proliferative and survival signaling, and the up‑regulation of angiogenic factors in endometrial stromal cells (6‑11). MIF binding notably induces the proteolytic cleavage of the CD74 intracellular domain which then promotes B cell differentiation (10). CD74 is up‑regulated on non‑immune cells at sites of inflammation including amyloid beta plaques and atherosclerotic plaques (12, 13). It is also up‑regulated in a variety of cancers and enhances tumorigenicity, tumor angiogenesis, and metastasis (1, 14).
- Beswick, E.J. and V.E. Reyes (2009) World J. Gastroenterol. 15:2855.
- Koch, N. et al. (1987) EMBO J. 6:1677.
- Riberdy, J.M. et al. (1992) Nature 360:474.
- Koch, N. et al. (1991) J. Immunol. 147:2643.
- Roche, P.A. et al. (1991) Nature 354:392.
- Leng, L. et al. (2003) J. Exp. Med. 197:1467.
- Takahashi, K. et al. (2009) Respir. Res. 10:33.
- Heinrichs, D. et al. (2011) Proc. Natl. Acad. Sci. 104:17444.
- Shi, X. et al. (2006) Immunity 25:595.
- Gore, Y. et al. (2008) J. Biol. Chem. 283:2784.
- Veillat, V. et al. (2010) J. Clin. Endocrinol. Metab. 95:E403.
- Bryan, K.J. et al. (2008) Mol. Neurodegen. 3:13.
- Martin-Ventura, J.L. et al. (2009) Cardiovasc. Res. 83:586.
- Liu, Y.-H. et al. (2008) J. Immunol. 181:6584.
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