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Recombinant rat IgG2a isotype controls are available. Condition of sample preparation and optimal sample dilution should be determined experimentally by the investigator.
Price/availability/specifications subject to change without notice. Unless otherwise indicated, our catalog and customized products are for research use only and not intended for human or animal diagnostic or therapeutic use.
Phone: 1-617-401-8149
Fax: 1-617-606-5019
Email: message@sydlabs.com
Or leave a message with a formal purchase
order (PO) Or credit card.
Recombinant Rat IgG2a Monoclonal Antibody.
Clone: RMT3-23.
Isotype: Rat IgG2a kappa.
Source: The anti-mouse CD366 (TIM-3) monoclonal antibody (clone: RMT3-23) was produced in mammalian cells.
Specificity/Sensitivity: The in vivo grade recombinant rat monoclonal antibody (clone: RMT3-23) specifically binds to mouse CD366 (TIM-3).
Applications: ELISA, neutralization, functional assays such as bioanalytical PK and ADA assays, and those assays for studying biological pathways affected by the mouse CD366 (TIM-3) protein.
Form of Antibody: 0.2 uM filtered solution, pH 7.4, no stabilizers or preservatives.
Endotoxin: < 1 EU per 1 mg of the protein by the LAL method.
Purity: >95% by SDS-PAGE under reducing conditions and HPLC.
Shipping: The in vivo grade recombinant anti-mouse CD366 (TIM-3) monoclonal antibody of clone RMT3-23 is shipped with ice pack. Upon receipt, store it immediately at the temperature recommended below.
Stability & 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 from date of receipt, 2 to 8°C as supplied.
Blockade of TIM3 relieves immunosuppression through reducing regulatory T cells in head and neck cancer.
Liu, J.-F., et al. J Exp Clin Cancer Res. 2018 Mar 5;37(1):44. doi: 10.1186/s13046-018-0713-7. PMID: 29506555
The prophylactic administration of isotype IgG2a (clone 2A3) or anti-TIM3 (RMT3–23) (BioXCell, West Lebanon, NH) in mice was carried out by intraperitoneal injections (100 μg i.p.) for 3 days since day 12 and then once a week for the following weeks. ...In the transgenic HNSCC mouse model, blockade of TIM3 by the anti-TIM3 monoclonal antibody induced a reduction of CD4+CD25+Foxp3+ Tregs. ...Meanwhile, the population of TIM3+ Tregs was also decreased. ...Interestingly, the percent of TIM3+ Tregs was also down-regulated in the anti-TIM3 therapy group (Fig. 4e). ...It suggested that TIM3 may participate in the differentiation of Tregs, and that the blockade of TIM3 induced a decline in the number of Tregs.
Tags: anti-mouse CD366 (TIM-3) RMT3-23; anti-mouse CD366 (TIM-3) RMT3-23 in vivo
Effect of TIM-3 Blockade on the Immunophenotype and Cytokine Profile of Murine Uterine NK Cells.
Tripathi, S., et al. PLoS One. 2015 Apr 21;10(4):e0123439. doi: 10.1371/journal.pone.0123439. PMID: 25897749
The treated group were injected i.p with anti TIM-3 mAb (clone RMT3-23, BioXCell) at doses 500μg, 250μg and 250μg at GD 6.5, 8.5 and 10.5 respectively. ...We determined if TIM-3 blockade significantly changes the cytokine and chemokine milieu at the FMI that affects the uNK cells. Allogeneically mated (CBA female x C57BL/6 male) female CBA mice treated with RMT3-23 (anti TIM-3) showed a decrease in the production of IL-6 (p = 0.0019), IL-15 (p = 0.0063) and IL-9 (p = 0.0128) in the placenta between G.D 10.5 and 12.5. ...The chemokine production in the placentae was also altered and a significant increase in the production of MIP1α (p = 0.0156), KC (murine equivalent of IL-8, p = 0.0276) and IP-10 (p = 0.0063) was observed in the placentae of RMT3-23 treated mice at G.D 10.5. ...We observed that TIM-3 is expressed on uNK cells and the number of uNK cells expressing TIM-3 increases steadily from GD 7.5 to 12.5, which is very similar to the expression of DBA on these cells. ...We used mAb RMT3-23 to block TIM-3 and observed the effect on the CD3 - CD122+ NK1.1 -DX5 - DBA+ cell population in the uteri at GD 7.5, 10.5 and 12.5.
Tags: anti-mouse CD366 (TIM-3) RMT3-23 antibody in mouse tumor model; bioactivity of anti-mouse CD366 (TIM-3) RMT3-23
A Threshold Level of Intratumor CD8+ T-cell PD1 Expression Dictates Therapeutic Response to Anti-PD1.
Ngiow, S. F., et al. Cancer Res. 2015 Sep 15;75(18):3800-11. doi: 10.1158/0008-5472.CAN-15-1082. PMID: 26208901
Purified anti-mouse PD1 mAb (RMP1-14), anti-mouse Tim3 (RMT3-23), anti-mouse PDL1 (10F.9G2), and control Ig (2A3) were purchased from BioXCell and used in the schedule and dose as indicated. ...We further confirmed our findings using a combination of anti-Tim3 and anti-PD1 mAbs in the CT26 tumor model, where a synergistic antitumor response of the combination was previously observed. ...The combination of anti-Tim3 and anti-PD1 mAbs induced a reduction in PD1+ intratumor CD8+ T cells consistent with the ability of anti-Tim3 to enhance an antitumor immune response toward CT26 via anti-PD1 therapy (Supplementary Fig. S5A and S5B). ...In contrast, consistent with no reduction in PD1+ T cells after the combination treatment of AT3 tumors (Supplementary Fig. S5C), anti-Tim3 and anti-PD1 mAb combination therapy was unable to suppress AT3 tumor growth (Supplementary Fig. S5D). ...We demonstrated that induction of intratumor Treg was, in part, a mechanism responsible for the development of anti-PD1–resistant tumors and PD1 hi CD8+ T cells.
Tags: anti-mouse CD366 (TIM-3) RMT3-23 of low endotoxin; anti-mouse CD366 (TIM-3) RMT3-23 antibody of low endotoxin
Antimetastatic effects of blocking PD-1 and the adenosine A2A receptor.
Mittal, D., et al. Cancer Res. 2014 Jul 15;74(14):3652-8. doi: 10.1158/0008-5472.CAN-14-0957. PMID: 24986517
Purified anti-mouse PD-1 mAb (RMP1-14), anti-mouse CTLA-4 mAb (UC10-4F10), anti-mouse Tim3 (RMT3-23) and control Ig (2A3) were purchased from BioXCell (West Lebanon) and used in the schedule and dose as indicated. ...Early treatment of B16F10-CD73 hi lung metastases by anti-CTLA-4, anti-PD-1, or anti-Tim3 mAb alone was relatively ineffective, compared with A 2ARi treatment alone over the same period. ...However, each of 3 checkpoint blockade mAbs, further enhanced the activity of A 2ARi when given coincidently in combination. ...on day 0 and 3 after tumor inoculation, mice were treated with intraperitoneal injections of vehicle, A 2ARi (SCH58261, 1 mg/kg), cIg (2A3, 250 μg), anti-CTLA-4 (UC10-4H10, 250 μg), anti-PD-1 (RMP1-14, 250 μg), anti-Tim3 (RMT3-23, 250 μg), or the combination as indicated. ...Total RNA was isolated from cancer cell lines and flow cytometry-sorted splenic lymphocytes by using RNAzol (Sigma-Aldrich) as per the manufacturer's instructions.
Tags: anti-mouse CD366 (TIM-3) antibody (RMT3-23); anti-mouse CD366 (TIM-3) RMT3-23
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, K. K., et al. PLoS Pathog. 2013;9(12):e1003798. doi: 10.1371/journal.ppat.1003798. PMID: 24339778
To block the Tim-3 pathway, 100 µg rat anti-mouse Tim-3 Ab (RMT3-23; BioXCell) was administered intraperitoneally every other day for 4 times. ...Another group of animals was injected with monoclonal antibodies against PD-L1 and Tim-3 to block inhibitory receptor signaling on CD8+ T cells. ...A 4-fold expansion of CD43+ CD8+ T cells was also found in mice treated with α-PD-L1 and α-TIM-3 but it was significantly lower than in the group of Treg depleted mice. ...Treg depletion resulted in a higher expansion of the total population of activated CD8+ T cells compared to inhibitory receptor blockage, whereas it was the other way around for the expansion of the tetramer+ cells recognizing the immunodominant FV CD8+ T cell epitope. ...This was also the case for the subset of tetramer+ CD8+ T cells but for these cells recognizing the immunodominant FV epitope the treatment with α-PD-L1 and α-TIM-3 was more efficient for granzyme B induction than Treg depletion.
Tags: clone RMT3-23 of anti-mouse CD366 (TIM-3) mAb; RMT3-23 anti-mouse CD366 (TIM-3) antibody
For more references about Anti-mouse CD366 (TIM-3) Monoclonal Antibody please contact our scientific support team with message@sydlabs.com.
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