Recombinant Human CD52 Fc Chimera Avi-tag Protein, CF Summary
Additional Information |
Biotinylated |
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant Human SIGLEC-10 Fc Chimera Protein
(Catalog #
2130-SL) is immobilized at 5.0 µg/mL (100 µL/well), the concentration of Biotinylated Recombinant Human CD52 Fc Chimera Avi-tag (Catalog # AVI9116) that produces 50% of the optimal binding response is 0.500-5.00 µg/mL. |
Source |
Chinese Hamster Ovary cell line, CHO-derived human CD52 protein Human CD52 (Gly25-Ser36) Accession # P31358.1 | IEGRMD | Human IgG1 (Pro100-Lys330) | Avi-tag | N-terminus | | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
Ser24 & Gly25 |
Structure / Form |
Disulfide-linked homodimer Biotinylated via Avi-tag |
Protein/Peptide Type |
Recombinant Proteins |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
30 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 |
38-44 kDa, under 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 with Trehalose. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 250 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 Human CD52 Fc Chimera Avi-tag Protein, CF
Background
CD52, also known as CAMPATH-1 antigen,
HE5, and gp20, is a cell surface glycoprotein that can be targeted to induce
immune suppression by complement-mediated cell lysis (1, 2). Mature human CD52
is a 12 amino acid peptide that is tethered to the cell surface with a GPI
linkage (3). It carries a large tissue-specific carbohydrate structure which
increases the molecular weight of CD52 to 15-20 kDa (3-5). CD52 is expressed on
lymphocytes, monocytes, monocycte-derived dendritic cells, eosinophils, and
neutrophils (6-8), as well as on mature spermatozoa and epithelial cells lining
the male genital tract (5, 9, 10). It protects sperm against anti-sperm
antibodies by binding to C1q and inhibiting complement activation (11). CD52
ligation on CD4+ T cells induces a suppressive population of cells that
release soluble CD52 which then binds to Siglec-10 (12-14). This interaction inhibits
the proliferation of activated T cells and the cytotoxic function of autoimmune
CD8+ T cells in type 1 diabetes (13). Our Avi-tag Biotinylated human CD52 Fc chimera features biotinylation at a single site contained within the Avi-tag, a unique 15 amino acid peptide. Protein orientation will be uniform when bound to streptavidin-coated surface due to the precise control of biotinylation and the rest of the protein is unchanged so there is no interference in the protein's bioactivity.
-
Morris, P.J. and N.K. Russell (2006) Transplantation 81:1361.
- Redpath, S. et al. (1998) Immunology 93:595.
- Xia, M.Q. et al. (1991) Eur. J. Immunol. 21:1677.
- Treumann, A. et al. (1995) J. Biol. Chem. 270:6088.
- Schroter, S. et al. (1999) J. Biol. Chem. 274:29862.
- Ratzinger, G. et al. (2003) Blood 101:1422.
- Elsner, J. et al. (1996) Blood 88:4684.
- Ambrose, L.R. et al. (2009) Blood 114:3052.
- Focarelli, R et al. (1998) Mol. Hum. Reprod. 4:119.
- Hale, G. et al. (1993) J. Reprod. Immunol. 23:189.
- Hardiyanto, L. et al. (2012) J. Reprod. Immunol. 94:142.
- Watanabe, T. et al. (2006) Clin. Immunol. 120:247.
- Bandala-Sanchez, E. et al. (2013) Nat. Immunol. 14:741.
- Toh, B.-H. et al. (2013) Cell. Mol. Immunol. 10:379.
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