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Recombinant Human NKG2E Fc Chimera Protein, CF

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When Recombinant Human CD94 (Catalog # 9270-CD) is coated at 1 μg/mL, Recombinant Human NKG2E Fc Chimera (Catalog # 9759-NK) binds with an ED50 of 1-7 μg/mL.

Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Human NKG2E Fc Chimera Protein, CF Summary

Details of Functionality
Measured by its binding ability in a functional ELISA. When Recombinant Human CD94 (Catalog # 9270-CD) is immobilized at 1 μg/mL, 100 μL/well, Recombinant Human NKG2E binds with an ED50 of 1-7 μg/mL.
Source
Human embryonic kidney cell, HEK293-derived human NKG2E protein
MDHuman IgG1
(Pro100-Lys330)
IEGRHuman NKG2E
(Glu98-Ser240)
Accession # Q07444-1
N-terminusC-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
  • Bioactivity
Theoretical MW
43 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
52-63 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 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 NKG2E Fc Chimera Protein, CF

  • killer cell lectin-like receptor subfamily C, member 3
  • NK cell receptor E
  • NKG2-E type II integral membrane protein
  • NKG2E
  • NKG2-E-activating NK receptor
  • NKG2ENKG2-E

Background

Human NKG2E (NK cell Group 2 isoform E; Killer cell lectin-like receptor subfamily C, member 3) is a member of the C-type lectin-like superfamily of proteins. Natural killer (NK) receptors are expressed in both NK cells and cytotoxic CD8+ T cells and have both activating and inhibitory members (1-3). Regulation of the balance between the activating and inhibitory receptors is important and lack of such regulation has been implicated in autoimmunity (4). The NKG2 family includes seven receptors: NKG2A, -B, -C, -D, -E, -F, and -H, which is the longer isoform of NKG2E. Except for NKG2D and NKG2F, the NKG2 family members form heterodimers with CD94 (5, 6). Human NKG2E consist of a 70 aa cytoplasmic domain, a 23 aa transmembrane segment, and a 147 aa extracellular domain (ECD). Within the ECD, human NKG2E shares 40% sequence identity with mouse NKG2E. NKG2E-CD94 heterodimers bind to the widely expressed nonclassical MHC-I molecule, HLA-E (Qa-1b in mouse), which presents a peptide derived from the signal peptide of classical MHC-I molecules (7, 8). Triggering the NKG2E-CD94 complex may activate the cytolytic activity and cytokine production of NK and CD8+ T cells (1, 7, 9). Over-expression of KLRC3/NKG2E in glioblastomas may play a major role in glioblastoma aggressiveness and recurrence (10).
  1. Orbelyan, G.A. et al. (2014) J. Immunol. 193:610.
  2. Tassi, I. et al. (2006) Immnunol Rev. 214:92.
  3. Lanier, L.L. (2008) Nat. Immunol. 9:495.
  4. Schleinitz, N. et al. (2010) Immunology. 174:2878.
  5. Lopez-Botet, M. et al. (2000) Hum. Immunol. 61:7.
  6. Braud, V.M. et al. (1998) Nature. 391:795.
  7. Vance, R.E. et al. (1999) J Exp Med 190:1801.
  8. Kaiser, B.K. et al. (2005) J Immunol 174:2878.
  9. Bellón, T. et al. (1999) J Immunol 162:3996.
  10. Cheray, M. et al. (2017) J Cell Mol Med 21:244.

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