>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Endotoxin Note
<0.01 EU per 1 μg of the protein by the LAL method.
Applications/Dilutions
Dilutions
Bioactivity
Theoretical MW
23.5 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
40-60 kDa, reducing conditions
Publications
Read Publication using 1885-TM in the following applications:
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 under reducing conditions and visualized by silver stain
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 Mouse TIM-2 Protein, CF
G9D3
T-cell immunoglobulin and mucin domain-containing protein 2
T-cell immunoglobulin mucin receptor 2
T-cell membrane protein 2
TIM2
TIM-2
TIMD-2
Background
T cell immunoglobulin and mucin domain‑2 (TIM‑2) is an approximately 50 kDa member of the TIM family of immune regulatory proteins. TIMs are type I transmembrane proteins with one Ig‑like V domain and a Ser/Thr‑rich mucin domain in their extracellular regions (1). Mature mouse TIM‑2 consists of a 210 amino acid (aa) extracellular domain (ECD), a 21 aa transmembrane segment, and a 53 aa cytoplasmic domain (2). Rat TIM‑2, by contrast, possesses the same structural architecture as mouse but contains an additional 46 aa within the mucin domain. Over comparable regions of the ECD, mouse and rat TIM‑2 share 74% aa sequence identity. The isolated ECD forms dimers and tetramers in solution, and these structures suggest the possibility of TIM‑2/TIM‑2 cis interactions (3). TIM‑2 is expressed on Th2 cells, B cells, oligodendrocytes, hepatocytes, hepatic stellate cells, and epithelial cells lining the bile duct and renal tubules (4 ‑ 9). It is upregulated on Th2 cells during cellular activation and functions as a negative regulator of Th2 cell expansion and immune responses (8 ‑ 11). TIM‑2 binds to ligands expressed on activated B cells, macrophages, dendritic cells, and T cells (8, 12). Its ligation by Semaphorin 4A induces tyrosine phosphorylation in the cytoplasmic domain of TIM‑2 (12). TIM‑2 binding to ligand(s) on hepatocytes inhibits hepatocyte differentiation and proliferation (7). TIM‑2 additionally plays a role in iron homeostasis by serving as an endocytic receptor for the heavy chain of Ferritin (H‑Ferritin) (4, 6).
Rodriguez-Manzanet, R. et al. (2009) Immunol. Rev. 229:259.
McIntire, J.J. et al. (2001) Nat. Immunol. 2:1109.
Santiago, C. et al. (2007) Immunity 26:299.
Todorich, B. et al. (2008) J. Neurochem. 107:1495.
Ruddell, R.G. et al. (2009) Hepatology 49:887.
Chen, T.T. et al. (2005) J. Exp. Med. 202:955.
Watanabe, N. et al. (2007) Hepatology 45:1240.
Chakravarti, S. et al. (2005) J. Exp. Med. 202:437.
Rennert, P.D. et al. (2006) J. Immunol. 177:4311.
Fukushima, A. et al. (2007) Immunol. Lett. 110:133.
Knickelbein, J.E. et al. (2006) J. Immunol. 177:4966.
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