Recombinant Human CD24 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 (Catalog #
2130-SL) is coated at 5 μg/mL, the concentration of Biotinylated Recombinant Human CD24 Fc Chimera Avi-tag (Catalog # AVI5247) that produces 50% optimal binding response is found to be approximately 1.5‑7.5 μg/mL. |
Source |
Chinese Hamster Ovary cell line, CHO-derived human CD24 protein Human CD24 (Ser27-Gly59) Accession # P25063.3 | IEGRMD | Human IgG1 (Pro100-Lys330) | Avi-tag | N-terminus | | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
Ser27 |
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 |
32 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 |
43-55 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 |
Supplied as a 0.2 μm filtered solution in PBS. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human CD24 Fc Chimera Avi-tag Protein, CF
Background
CD24, also known as Heat-Stable Antigen and Nectadrin,
is a heavily and variably glycosylated 30 kDa-60 kDa
GPI-linked sialoprotein (1-4). Human CD24 is expressed on B lineage cells and
granulocytes, on epithelial, neuronal, and muscle cells, and on a range of
tumor cells (4-6). In mouse, CD24 is even more widely expressed, particularly
on T cells, monocytes, and dendritic cells (2). CD24 expression is regulated
during lineage development and with the activation of various cell types (4).
Antibody crosslinking of CD24 enhances the induction of apoptosis in B and T
lymphocytes which contributes to negative selection and the induction of immune
tolerance (7-11). CD24 on antigen presenting cells cooperates with B7
molecules in the co-stimulation of T cells (12-14). CD24 associates
in cis
with Siglec-10 (or Siglec-G in mouse) and with the danger-associated molecules
HMGB1, HSP70, or HSP90 which are released from necrotic or damaged cells (15).
Formation of these ternary complexes fills a protective role: the resulting
Siglec-10 signaling inhibits inflammatory responses that are otherwise induced
by extracellular DAMPs (15, 16). Mature human CD24 shares 30% and 42%
amino acid sequence identity with mouse and rat CD24, respectively. Our Avi-tag
Biotinylated human CD24 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.
- Jackson, D. et al. (1992) Cancer Res. 52:5264.
- Kay, R. et al. (1991) J. Immunol. 147:1412.
- Kadmon, G. et al. (1992) J. Cell Biol. 118:1245.
- Fang, X. et al. (2010) Cell. Mol. Immunol. 7:100.
- Fischer, G. F. et al. (1990) J. Immunol. 144:638.
- Allman, D.M. et al. (1993) J. Immunol. 151:4431.
- Suzuki, T. et al. (2001) J. Immunol. 166:5567.
- Taguchi, T. et al. (2003) J. Immunol. 170:252.
- Jung, K.C. et al. (2004) J. Immunol. 172:795.
- Kishimoto, H. and J. Sprent (1997) J. Exp. Med. 185:263.
- Hitsumoto, Y. et al. (1996) Immunology 89:200.
- Liu, Y. et al. (1992) Eur. J. Immunol. 22:2855.
- Enk, A.H. and S.I. Katz (1994) J. Immunol. 152:3264.
- Askew, D. and C.V. Harding (2008) Immunology 123:447.
- Chen G.Y. et al. (2009) Science 323:1722.
- Liu, Y. et al. (2011) Curr. Opin. Immunol. 23:41.
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