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MABF230

Sigma-Aldrich

Anti-TIM-3, clone RMT3-23, Azide Free Antibody

clone RMT3-23, from rat

同義詞:

Hepatitis A virus cellular receptor 2 homolog, HAVcr-2, T-cell immunoglobulin and mucin domain-containing protein 3, TIMD-3, T-cell immunoglobulin mucin receptor 3, TIM-3, T-cell membrane protein 3

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About This Item

分類程式碼代碼:
12352203
eCl@ss:
32160702
NACRES:
NA.41

生物源

rat

品質等級

抗體表格

purified immunoglobulin

抗體產品種類

primary antibodies

無性繁殖

RMT3-23, monoclonal

物種活性

mouse

技術

flow cytometry: suitable
immunocytochemistry: suitable
immunohistochemistry: suitable
western blot: suitable

同型

IgG2aκ

NCBI登錄號

UniProt登錄號

運輸包裝

wet ice

目標翻譯後修改

unmodified

基因資訊

mouse ... Havcr2(171285)

一般說明

The protein called Hepatitis A virus cellular receptor 2 (HAVcr-20), T-cell immunoglobulin and mucin domain-containing protein 3 (TIMD-3), T-cell immunoglobulin mucin receptor 3 (TIM-3), or T-cell membrane protein 3 and encoded by the human gene HAVCR2/TIM3/TIMD3 is an important protein in the regulation of macrophage activation. TIM-3 is also critical for immune tolerance as it inhibits T-helper type 1 (Th1) mediated auto and alloimmune responses. Finally TIM-3 plays an important role in T-cell homing in the thymus and lymph and is the receptor for the Galectin-9 an important protein modulating cell-cell and cell matrix interactions. TIM-3 is a membrane bound protein that is expressed largely by immune system cells. High TIM-3 expression is also associated with many tumors including renal cancer and acute myelogenous leukemia (AML), and its expression is also a target for anti-cancer therapy as anti-TIM-3 antibodies have been shown to eradicate leukemic stem cells (LSCs) in animal models of AML.

免疫原

Recombinant protein corresponding to mouse TIM-3.

應用

Inhibits Activity/Function Assay: Co-administration of a representative lot by an independent laboraotory with FVAX significantly suppressed tumor growth to a greater extent than FVAX alone. Treatment with Anti-TIM-3 , clone RMT3-23, Azide Free also augmented antitumor activities of plasmid DNA encoding melanoma target gp100 or TRP2, suggesting that targeting TIM-3 or TIM-4 improves antitumor activiites of other forms of cancer vaccines. (Bagdadi, M., et al. (2013). Cancer Immunol Immunother. 62(4):629-637.).

Flow Cytometry Analysis: 1 µg from a representative lot detected TIM-3 in TIM-3 transfected 1X10E6 BALB/L5178Y cells.

Flow Cytometry Analysis: A representative lot detected TIM-3 in dendritic cells, macrophages, splenocytes, and hepatic mononuclear cells from acute graft-vs-host disease (aGVHD) mice (Oikawa, T., et al. (2006). J Immunol. 177(7):4281-4287.).

Immunohistochemistry Analysis: A representative lot from an independent laboratory detected TIM-3 in liver tissue from normal and aGVHD mice (Oikawa, T., et al. (2006). J Immunol. 177(7):4281-4287.).

Immunocytochemistry Analysis: A representative lot from an independent laboratory detected TIM-3 in HMGB1-deficient MEF cells (Chiba, S., et al. (2012). Nat Immunol. 13(9):832-842.).
This Anti-TIM-3 antibody, clone RMT3-23, Azide Free is validated for use in western blotting, flow cytometry, IHC, ICC & Inhibits activity/Function for the detection of TIM-3.

品質

Evaluated by Western Blotting in TIM-3 transfected L5178Y cell lysate.

Western Blotting Analysis: 1 µg/mL of this antibody detected TIM-3 in 10 µg of TIM-3 transfected L5178Y cell lysate.

標靶描述

~31 kDa observed

外觀

Format: Purified
Purified rat monoclonal IgG2aκ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl without preservatives.

其他說明

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

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儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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Preferential involvement of Tim-3 in the regulation of hepatic CD8+ T cells in murine acute graft-versus-host disease.
Oikawa, Tsunekazu, et al.
Journal of immunology (Baltimore, Md. : 1950), 177, 4281-4287 (2006)
Combined blockade of TIM-3 and TIM-4 augments cancer vaccine efficacy against established melanomas.
Baghdadi, Muhammad, et al.
Cancer Immunology, Immunotherapy, 62, 629-637 (2013)
Shigeki Chiba et al.
Nature immunology, 13(9), 832-842 (2012-07-31)
The mechanisms by which tumor microenvironments modulate nucleic acid-mediated innate immunity remain unknown. Here we identify the receptor TIM-3 as key in circumventing the stimulatory effects of nucleic acids in tumor immunity. Tumor-associated dendritic cells (DCs) in mouse tumors and

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