Recombinant Mouse IGSF2/CD101 Fc Chimera Protein, CF Summary
Details of Functionality |
Measured by its ability to inhibit anti-CD3-induced proliferation of stimulated human T cells. The ED50 for this effect is 1.4-8.4 μg/mL.
|
Source |
Mouse myeloma cell line, NS0-derived mouse IGSF2/CD101 protein Mouse CD101 (Gln21-Phe974) Accession # A8E0Y8 | IEGRMDP | Mouse IgG2a (Glu98-Lys330) | N-terminus | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
No results obtained. Gln21 inferred from enzymatic pyroglutamate treatment revealing Arg22.
|
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. |
Purity Statement |
Antigen Affinity-purified |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
133 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 |
121-150 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 °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 400 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 IGSF2/CD101 Fc Chimera Protein, CF
Background
CD101, also known as Immunoglobulin Superfamily member 2
(IGSF2) or cell surface glycoprotein V7 (V7), is a 130-145 kDa type 1
transmembrane glycoprotein within the very large Ig superfamily (1). Ig
superfamily members participate in diverse functions including cell-cell
recognition and adhesion, soluble molecules and specific antigen recognition,
and are grouped based on the presence of a characteristic Ig domain fold. Mature mouse CD101 consists of a large
extracellular domain (ECD) containing a Glu-Trp-Ile (EWI) motif and 7 Ig-like
V-type domains, a single transmembrane domain, and a short cytoplasmic domain
(1, 2). The mouse CD101 ECD shares 71% and 87% amino acid sequence identity
with human and rat CD101 ECD, respectively. The exact biological functions,
interacting ligands and mode of signal transduction for CD101 currently remain
unclear. CD101 expression has been found on dermal dendritic cells (DCs),
granulocytes, monocytes, activated T cells, and CD4
+ CD25
+
FoxP3
+ T regulatory cells (Tregs) (2-5). CD101 expression has been
linked to immune suppression by Tregs in humans (6), with ligation of CD101 on
DCs inducing IL-10 expression (2) and ligation on activated T cells blocking
IL-2 expression (7). Both of these effects down-regulate T cell activity. Notably, in mice, CD101
expression on CD62L
++ Tregs identifies a population of cells
that have potent suppressor activity (5). In humans, reduced CD101 expression
on mucosal CD8
+ T cells has been linked to increased tissue
inflammation in both intestinal (8) and pulmonary mucosa (9). In both mouse and
human, mutations in CD101 have been associated with increased susceptibility for
diabetes (10, 11). CD101 expression may act as a potential
biomarker for CD4
+ CD56
+ blastic tumors (12) and
inflammatory bowel disease activity (13), and missense variants of its gene
have been associated with increased risk of HIV-1 acquisition (14).
- Stipp, C. et al. (2001) J. Biol. Chem. 276:40545.
- Bouloc, A. et al. (2000) Eur. J. Immunol. 30:3132.
- Rivas, A. et al. (1995) J. Immunol. 154:4423.
- Ruegg, C. et al. (1995) J. Immunol. 154:4434-CD.
- Fernandez, I. et al. (2007) J. Immunol. 179:2808.
- Hua, J. et al. (2015) J. Immunol. 195:3642.
- Soares, L. et al. (1998) J. Immunol. 161:209.
- Brimnes, J. et al. (2005) J. Immunol. 174:5814.
- Kumar, B. et al. (2017) Cell Rep. 20:2921.
- Rainbow, D. et al. (2011) J Immunol. 187:325.
- Okuno, M. et al. (2017) J Diabetes Investig. 8:286.
- Meyer, N. et al. (2005) J. Invest. Dermatol. 124:668.
- Schey, R. et al. (2016) Mucosal Immunol. 9:1205.
- Mackelprang, R. et al. (2017) PLoS Pathog. 13:e1006703.
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