Recombinant Human CD45RO Fc Chimera Protein, CF Summary
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant Human CD45RO (Catalog # 10642-CD) is immoblized at 2 µg/mL (100 µL/well), the concentration of Recombinant Human Galectin-1 Protein
(Catalog #
1152-GA) that produces a 50% optimal binding response is found to be 100-500 ng/mL. |
Source |
Chinese Hamster Ovary cell line, CHO-derived human CD45RO protein Human CD45RO (Gln24-Lys391) Accession # BAF84820.1 | IEGRMD | Human IgG1 (Pro100-Lys330) | N-terminus | | C-terminus | |
|
Accession # |
|
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 |
71 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 |
114-132 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. |
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 CD45RO Fc Chimera Protein, CF
Background
CD45, previously called LCA (leukocyte common antigen), T200, or Ly5 in
mice, is member C of the class 1 (receptor‑like) protein
tyrosine phosphatase family (PTPRC) (1, 2). It is a variably glycosylated 180-220 kDa transmembrane protein that is
abundantly expressed on all nucleated cells of hematopoietic origin (1-3).
Multiple splicing isoforms of exon 4 (A), 5 (B), and 6 (C) are expressed
according to cell type, developmental stage and antigenic exposure (1-5). The
longest form, CD45RABC (called B220 in mouse) is expressed on
B lymphocytes, The shortest form, CD45R0, lacking exons 4, 5 and 6 which encode aa 34‑194, is expressed on
memory cells, while intermediate sizes are expressed on other T cells (3, 4,
6). Human CD45 has a 40% and 41% sequence identity with mouse and rat
respectively. The CD45R0 cDNA encodes 1145 amino acids (aa), including a 25 aa
signal sequence, a 391 aa extracellular domain, 21 aa transmembrane sequence,
and a 708 aa cytoplasmic domain that contains two phosphatase domains, D1 and
D2. Only D1 has phosphatase activity. CD45 has been best studied in T cells,
where it determines T cell receptor signaling thresholds (3, 6‑8). CD45 is moved
into or out of the immunological synapse (IS) membrane microdomain depending on
the relative influence of interaction with the extracellular galectin lattice
or the intracellular actin cytoskeleton (9, 10). Galectin interaction can be
fine‑tuned by varying usage of the heavily O‑glycosylated spliced
regions and sialylation of N‑linked carbohydrates
(4, 9). Within the IS, CD45 dephosphorylates and negatively regulates the Src
family kinase, Lck (8‑10). In other
leukocytes, CD45 influences differentiation and links immunoreceptor signaling
with cytokine secretion and cell survival, partially overlapping in function
with DEP‑1/CD148 (11‑14). CD45 deletion
causes in severe immunodeficiency, while point mutations may be associated with
autoimmune disorders (6, 7).
- Anderson, J.N. et al. (2004) FASEB J. 18:8.
- Streuli, M. et al. (1987) J. Exp. Med. 166:1548.
- Hermiston, M.L. et al. (2003) Annu. Rev. Immunol. 21:107.
- Earl, L.A. and L.G. Baum (2008) Immunol. Cell Biol. 86:608.
- Ralph, S.J. et al. (1987) EMBO J. 6:1251.
- Falahti, R. and D. Leitenberg (2008) J. Immunol. 181:6082.
- Tchilian, E.Z. and P.C.L. Beverley (2006) Trends Immunol. 27:146.
- McNiell, L. et al. (2007) Immunity 27:425.
- Chen, I-J. et al. (2007) J. Biol. Chem. 282:35361.
- Freiberg, B.A. et al. (2002) Nat. Immunol. 3:911.
- Zhu, J.W. et al. (2008) Immunity 28:183.
- Huntington, N.D. et al. (2006) Nat. Immunol. 7:190.
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