Anti-Mouse TIM-3 (Clone B8.2C12) - Biotin - 500 µg

2 - 8°C Wet Ice

TIM-3 is a member of the T cell immunoglobulin mucin gene family and encodes a type Imembrane protein consisting of an immunoglobulin variable-region-like domain, a mucin-likedomain, and a tyrosine phosphorylation motif1. TIM-3 functions as an important immune checkpoint receptor that helps regulate dendritic cell function2, T helper type I expansion, and induction of peripheral tolerance3. TIM-3 interacts with GAL-9, PtdSer, HMGB1 and CEACAM1 to activate biochemical pathways such as immune tolerance, T cell depletion, NF-κB signaling, and IL-2 secretion4. Additionally, TIM-3 expression correlates with terminal differentiation and exhaustion in tumors as well as chronic infection3. Due to its dysregulation in different types of cancer, TIM-3 blockade is being investigated as an anti-tumor immunotherapy2, 4. TIM-3 also has potential as a prognostic marker in solid tumors4.B8.2C12 was generated by immunizing Lewis and Lou/M female rats (Harlan Sprague-Dawley)with Th1 polarized T cell clones and/or lines, including Th1-specific clone AE7 and in vitrodifferentiated Th1 cell lines derived from 5B6 and DO11.10 T cell receptor transgenic mice1. Spleen cells were fused with myeloma cells and a large panel of monoclonal antibodies was screened on Th1 and Th2 cells by flow cytometry. B8.2C12 selectively stained Th1 cells. Gene expression cloning was then used to identify a complementary DNA, which was TIM-3.

0.5 mg/ml

TIM-3 (CD366) is expressed on interferon-γ producing T cells, dendriticcells, cytotoxic lymphocytes, exhausted T cells, natural killer cells, Th17, and myeloid cells.TIM-3 is also expressed on CD8 + T cells in the tumor microenvironment as well as intratumoralmacrophages and monocytes. TIM-3 is expressed by T helper 1 cells after several rounds ofpolarization in vitro. TIM-3 is not expressed by naïve T cells.