Recombinant Human ULBP-2 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 NKG2D/CD314 Fc Chimera
(Catalog #
1299-NK) is immobilized at 0.5
µg/mL (100 µL/well), Biotinylated Recombinant Human ULBP-2 Fc Chimera Avi-tag (Catalog
# AVI1298) binds with an ED 50 of 0.500-8.00 ng/mL. |
Source |
Chinese Hamster Ovary cell line, CHO-derived human ULBP-2 protein Human ULBP-2 (Gly26-Ser217) Accession # Q9BZM5.1 | IEGRMD | Human IgG1 (Pro100-Lys330) | Avi-tag | N-terminus | | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
Gly26 |
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 |
50 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 |
60-70 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 ULBP-2 Fc Chimera Avi-tag Protein, CF
Background
ULBP-2 is a member of a family of cell-surface
proteins that function as ligands for human NKG2D. ULBP-2 has also been
described under the names RaeT1H (retinoic acid early transcript), NKG2DL2, and
ALCAN-alpha. The name ULBP-2 derives from the original identification of three
proteins, ULBP-1, -2, and -3, as ligands for the human cytomegalovirus
glycoprotein UL16; they were designated UL16 binding proteins (ULBP). The gene
for ULBP-2 resides in a cluster of ten related genes, six of which encode
potentially functional glycoproteins. Amino acid sequence identity within this
family ranges from 30-60%. These proteins are distantly related to MHC class
I proteins, but they possess only the alpha 1 and alpha 2 Ig-like domains, and
they have no capacity to bind peptide or interact with beta 2-microglobulin.
Some family members, including ULBP-2, are anchored to the membrane via a
GPI-linkage, whereas others have transmembrane domains. ULBP-2 and several
other family members are known to bind to human NKG2D, an activating receptor
expressed on NK cells, NKT cells, gamma δ T cells, and CD8+ alpha
beta T cells. Engagement of NKG2D results in the activation of cytolytic
activity and/or cytokine production by these effector cells. The ULBPs are
expressed on some tumor cells and have been implicated in tumor surveillance. Our Avi-tag Biotinylated Recombinant Human ULBP-2
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.
- Cosman, D. et al. (2001) Immunity 14:123.
- Kubin, M. et al. (2001) Eur. J. Immunol. 31:1428.
- Sutherland, C. et al. (2002) J. Immunol. 168:671.
- Steinle, A. et al. (2001) Immunogenetics 53:279.
- Sutherland, C. et al. (2001) Immunol. Rev. 181:185.
- Pende, D. et al. (2002) Cancer Res. 62:6178.
- Radosavljevic, M. et al. (2002) Genomics 79:114.
- NKG2D and its Ligands (2002) www.rndsystems.com.
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