Recombinant Cynomolgus CD96 His-tag Protein, CF Summary
| Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant Cynomolgus Monkey CD96 His-tag (Catalog # 10478-CD) is immobilized at 1 µg/mL (100 µL/well), Recombinant Recombinant Human CD155/PVR Fc Chimera
(Catalog #
9174-CD) binds with an ED 50 of 6-36 ng/mL. |
| Source |
Human embryonic kidney cell, HEK293-derived cynomolgus monkey CD96 protein Lys25-Met503, with a C-terminal 6-His tag |
| Accession # |
|
| N-terminal Sequence |
Lys25 |
| 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 |
54 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 |
120-145 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 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 Cynomolgus CD96 His-tag Protein, CF
Background
CD96,
also known as Tactile (T cell-activated increased late expression), is a type I
transmembrane glycoprotein belonging to the Ig superfamily that shows peak
expression 6-9 days after activation of T, NK, and a subpopulation of B cells
(1, 2). The extracellular domain (ECD)
of CD96 contains three highly N- and O‑glycosylated Ig-like domains, with the
two N-terminal domains being V-type and the distal domain a C-type structure
(1). Within the mature ECD, cynomolgus
CD96 shares 87% and 54% amino acid sequence identity with human and mouse CD96,
respectively. In human, a splice variant
with a 16 aa deletion in the second V-type domain, called CD96v2, can be
expressed (2). CD96 is frequently expressed on acute myeloid leukemia and
myelodysplastic stem cells (3, 4). It is also expressed on CD4+ and CD8+ T
cells, plus NK cells and select B cells (5). Low expression of adhesive human CD96
is a rare cause of C syndrome, a set of developmental anomalies in cranial bone
(trigonocephaly), skin and viscera, demonstrating a role for CD96 in
development of these tissues (2, 6). An 80 kDa soluble form is elevated in
human serum during chronic hepatitis B (9). The most N-terminal Ig-like domain
of human CD96 binds to CD155/PVR (poliovirus receptor), but CD96/CD155
interaction is species-specific (2, 7, 10). On NK cells, co-stimulatory CD96
and DNAM-1 (CD226) are thought to have paired activity with inhibitory TIGIT,
all of which bind CD155 and various nectins (11, 12). CD96 can promote NK cell
adhesion to, and killing of target cells, including tumors that express CD155
(10, 11).
- Wang, P.L. et al. (1992) J. Immunol. 148:2600.
- Meyer, D. et al. (2009) J. Biol. Chem. 284:2235.
- Hosen, N. et al. (2007) Proc. Natl. Acad. Sci. USA 104:11008.
- Xie, W. et al. (2010) Cytometry A 77:840.
- Eriksson, E. M. et al. (2012) PLOS One 7:e51696.
- Kaname, T. et al. (2007) Am. J. Hum. Genet. 81:835.
- Seth, S. et al. (2007) Biochem. Biophys. Res. Commun. 364:959.
- Protein Accession # BAE32358.
- Gong, J. et al. (2008) Clin. Exp. Immunol. 155:207.
- Fuchs, A. et al. (2004) J. Immunol. 172:3394.
- Stanietsky, N. and O. Mandelboim (2010) FEBS Lett. 584:4895.
- Xu, Z. and B. Jin (2010) Cell. Mol. Immunol. 7:11.
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