Product image
InVivoMAb anti-mouse TIM-3 (CD366)
BE0115
ApplicationsFlow Cytometry, Neutralisation/Blocking
Product group Antibodies
ReactivityMouse
Overview
- SupplierBio X Cell
- Product NameInVivoMAb anti-mouse TIM-3 (CD366)
- Delivery Days Customer7
- ApplicationsFlow Cytometry, Neutralisation/Blocking
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone IDRMT3-23
- Concentration4-11 mg/ml
- Estimated Purity>95%
- HostRat
- IsotypeIgG2a
- ReactivityMouse
- Storage Instruction2°C to 8°C
- UNSPSC12352203
References
- Blockade of TIM3 relieves immunosuppression through reducing regulatory T cells in head and neck cancer. Liu JF et al., 2018 Mar 5, J Exp Clin Cancer ResRead more
- TIGIT predominantly regulates the immune response via regulatory T cells. Kurtulus S et al., 2015 Nov 2, J Clin InvestRead more
- A Threshold Level of Intratumor CD8+ T-cell PD1 Expression Dictates Therapeutic Response to Anti-PD1. Ngiow SF et al., 2015 Sep 15, Cancer ResRead more
- Effect of TIM-3 Blockade on the Immunophenotype and Cytokine Profile of Murine Uterine NK Cells. Tripathi S et al., 2015, PLoS OneRead more
- Programmed death-1 impairs secondary effector lung CD8+ T cells during respiratory virus reinfection. Erickson JJ et al., 2014 Nov 15, J ImmunolRead more
- Antimetastatic effects of blocking PD-1 and the adenosine A2A receptor. Mittal D et al., 2014 Jul 15, Cancer ResRead more
- Liver-primed CD8+ T cells suppress antiviral adaptive immunity through galectin-9-independent T-cell immunoglobulin and mucin 3 engagement of high-mobility group box 1 in mice. Dolina JS et al., 2014 Apr, HepatologyRead more
- Combining regulatory T cell depletion and inhibitory receptor blockade improves reactivation of exhausted virus-specific CD8+ T cells and efficiently reduces chronic retroviral loads. Dietze KK et al., 2013, PLoS PathogRead more
- Immunotherapy-induced CD8+ T cells instigate immune suppression in the tumor. McGray AJ et al., 2014 Jan, Mol TherRead more
- Virus-specific CD8+ T cells upregulate programmed death-1 expression during acute friend retrovirus infection but are highly cytotoxic and control virus replication. Zelinskyy G et al., 2011 Oct 1, J ImmunolRead more