Recombinant Mouse NKG2A (CHO-expressed) Fc Protein, CF Summary
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant Mouse NKG2A/CD159a Fc Chimera is coated at 0.5 µg/mL, recombinant human CD94
binds with a typical ED50 of 0.1-0.6 μg/mL. |
Source |
Chinese Hamster Ovary cell line, CHO-derived mouse NKG2A/CD159a protein MDP | Mouse IgG2A (Glu98-Lys330) | IEGR | Mouse NKG2A (Ala94-IIe244) Accession # Q9Z202 | N-terminus | | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
Met |
Structure / Form |
Disulfide-linked homodimer |
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 |
44 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 |
58-67 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 visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 500 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 NKG2A (CHO-expressed) Fc Protein, CF
Background
NKG2A/CD159a is an approximately 40 kDa transmembrane C-type lectin superfamily protein that inhibits innate immune system activation (1). Mouse NKG2A consists of a 70 amino acid (aa) cytoplasmic domain with two ITIM inhibitory motifs, a 23 aa transmembrane segment, and a 151 aa extracellular domain (ECD) with one C-type lectin domain (2). Within the ECD, mouse NKG2A shares 41% and 71% aa sequence identity with human and rat NKG2A, respectively. Alternative splicing generates additional isoforms with a 17 aa deletion in the extracellular juxtamembrane region or a substitution of that region plus the transmembrane segment. NKG2A is expressed on a subset of NK cells and CD8
+ T cells (2-6) where it forms a covalent heterodimer with CD94 (5, 7, 8). NKG2A-CD94 heterodimers bind to the widely expressed nonclassical MHC-I molecule, HLA-E (Qa-1
b in mouse), which presents a peptide derived from the signal peptide of classical MHC-I molecules (2, 7). Triggering the NKG2A-CD94 complex inhibits the cytolytic activity of NK and CD8
+ T cells (2, 3, 5, 6, 9). This enables the innate immune system to detect cells that express host MHC-I molecules and to protect them from NK cell mediated lysis. This mechanism is subverted by human cytomegalovirus which encodes a peptide that is homologous to the HLA-E binding peptide (10). HCMV infected cells up-regulate both HLA-E and NKG2A expression and utilize this peptide to escape from immune clearance (3, 10). In contrast, vaccinia virus induces HLA-E down-regulation, thus permitting NK cell lysis of the virally infected cell (11).
- Das, J. and S.I. Khakoo (2015) Immunol. Rev. 267:214.
- Vance, R.E. et al. (1998) J. Exp. Med. 188:1841.
- Saez-Borderias, A. et al. (2009) J. Immunol.182:829.
- Houchins, J.P. et al. (1997) J. Immunol. 158:3603.
- Brooks, A.G. et al. (1997) J. Exp. Med. 185:795.
- Zhou, J. et al. (2008) J. Immunol. 180:25.
- Braud, V.M. et al. (1998) Nature 391:795.
- Carretero, M. et al. (1997) Eur. J. Immunol. 27:563.
- Lee, N. et al. (1998) Proc. Natl. Acad. Sci. USA 95:5199.
- Tomasec, P. et al. (2000) Science 287:1031.
- Brooks, C.R. et al. (2006) J. Immunol. 176:1141.
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