Recombinant Rat B7-H2 Fc Chimera Protein, CF Summary
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant Rat B7-H2 Fc Chimera (Catalog # 10419-B7) is Immobilized at 1.0 μg/mL (100 μL/well), the concentration of Recombinant Mouse ICOS Fc Chimera
(Catalog #
168-CS)
that produces 50% optimal binding response is found to be approximately 10-100 ng/mL. |
Source |
Mouse myeloma cell line, NS0-derived rat B7-H2 protein Rat B7-H2 (Glu25-Lys261) Accession # XP_006256322.1 | IEGRMD | Human IgG1 (Pro100-Lys330) | N-terminus | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
Glu25 |
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 |
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 |
70-90 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. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 200 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 Rat B7-H2 Fc Chimera Protein, CF
Background
B7-H2,
also known as B7-related protein 1 (B7RP1), ICOS Ligand, and CD275, is an
approximately 60 kDa type I transmembrane glycoprotein in the
B7 family of immune regulatory molecules (1). Within the extracellular
domain, rat B7-H2 shares 70% and 54% amino acid (aa) sequence identity with mouse and human
B7‑H2, respectively. Alternative splicing generates
a long isoform that carries a 10 aa substitution for the 3 C-terminal
residues in humans and a 27 aa substitution for the 2 C-terminal residues
in mouse. B7-H2 is expressed on antigen
presenting cells such as B cells, macrophages, monocytes, and dendritic
cells
(2-6). B7-H2 binds to ICOS on activated T cells, leading to both positive
and negative effects on immune responses including its own down-regulation
(2, 4, 7). Rat and human B7-H2 exhibit cross-species binding to ICOS
(3, 6). The B7-H2 interaction with ICOS is co-stimulatory for T cell
proliferation as well as the development of B cells, plasma cells,
follicular helper T cells (Tfh) and germinal centers (2-4, 8, 9). In human
but not in mouse, B7-H2 additionally binds to CD28 and CTLA4, and its
interaction with CD28 can co-stimulate both human and mouse naïve T cells
and regulatory T cells (Treg) (6). B7-H2 contributes to the development of
allergic asthma by enhancing Th2 biased immune responses, limiting Th17
responses, and promoting eosinophilic infiltration into the lung
(8, 10, 11). Its activation of ICOS on Treg limits pulmonary
inflammation and airway hyperresponsiveness, promotes the development of
inhalational tolerance, and impairs anti-tumor immunity (5, 12, 13).
In contrast, its ligation of ICOS on Tfh cells can increase the severity of
autoimmune symptoms (9). A soluble form of human B7-H2 is elevated in the
circulation of patients with active systemic lupus erythematosus (14). In the
thyroid, B7-H2 is up-regulated on thyrocytes during inflammation and promotes
their proliferation and production of thyroid hormones (15). B7-H2 and ICOS are also
expressed on ILC2 cells. B7-H2/ICOS interaction promoted cytokine production
and survival in ILC2 cells through STAT5, suggesting that B7-H2/ICOS signaling
pathway is critically involved in ILC2 function and homeostasis (16).
- Bour-Jordan, H. et al. (2011) Immunol. Rev. 241:180.
- Wang, S. et al. (2000) Blood 96:2808.
- Yoshinaga, S.K. et al. (2000) Int. Immunol. 12:1439.
- Yoshinaga, S.K. et al. (1999) Nature 402:827.
- Faget, J. et al. (2012) Cancer Res. 72:6130.
- Yao, S. et al. (2011) Immunity 32:729.
- Watanabe, M. et al. (2008) J. Immunol. 180:5222.
- Wong, S.-C. et al. (2003) Blood 102:1381.
- Hu, Y.-L. et al. (2009) J. Immunol. 182:1421.
- Kadkhoda, K. et al. (2010) J. Immunol. 184:3780.
- Kadkhoda, K. et al. (2011) Int. Immunol. 23:239.
- Gajewska, B.U. et al. (2005) J. Immunol. 174:3000.
- Akbari, O. et al. (2002) Nat. Med. 8:1024.
- Her, M. et al. (2009) Lupus 18:501.
- Wang, F. et al. (2012) J. Clin. Immunol. 32:1253.
- Maazi H. et al. (2015) Immunity. 42:538.
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