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Anti-TIM-3 Antibody

Mouse Monoclonal Antibody specific to TIM3

Product Specifications

CAS Number

9007-83-4

Product Name Alternative

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, CD antigen CD366

Gene Name

HAVCR2

NCBI Gene ID

<a href="https://www.ncbi.nlm.nih.gov/gene/?term=HAVCR2">HAVCR2</a>

UniProt

Q8TDQ0

Cellular Locus

Membrane, Cell junction, Cell membrane

Host

Mouse

Reactivity

Human

Immunogen

Recombinant human TIM-3.

Target Antigen

Hepatitis A virus cellular receptor 2

Target

TIM-3

Clonality

Monoclonal

Isotype

IgG1

Type

Antibody

Applications

IHC

Field of Research

Cancer research

Purification Method

Purified by immunoaffinity chromatography

Concentration

Lot Specific

Dilution

Dilute in PBS or medium that is identical to that used in the assay system.

Format

Purified

Form

Liquid

Buffer

Tris

Function

Cell surface receptor implicated in modulating innate and adaptive immune responses. Generally accepted to have an inhibiting function. Reports on stimulating functions suggest that the activity may be influenced by the cellular context and/or the respective ligand (PubMed:24825777). Regulates macrophage activation (PubMed:11823861). Inhibits T-helper type 1 lymphocyte (Th1)-mediated auto- and alloimmune responses and promotes immunological tolerance (PubMed:14556005). In CD8+ cells attenuates TCR-induced signaling, specifically by blocking NF-kappaB and NFAT promoter activities resulting in the loss of IL-2 secretion. The function may implicate its association with LCK proposed to impair phosphorylation of TCR subunits, and/or LGALS9-dependent recruitment of PTPRC to the immunological synapse (PubMed:24337741, PubMed:26492563). In contrast, shown to activate TCR-induced signaling in T-cells probably implicating ZAP70, LCP2, LCK and FYN (By similarity). Expressed on Treg cells can inhibit Th17 cell responses (PubMed:24838857). Receptor for LGALS9 (PubMed:16286920, PubMed:24337741). Binding to LGALS9 is believed to result in suppression of T-cell responses; the resulting apoptosis of antigen-specific cells may implicate HAVCR2 phosphorylation and disruption of its association with BAG6. Binding to LGALS9 is proposed to be involved in innate immune response to intracellular pathogens. Expressed on Th1 cells interacts with LGALS9 expressed on Mycobacterium tuberculosis-infected macrophages to stimulate antibactericidal activity including IL-1 beta secretion and to restrict intracellular bacterial growth (By similarity). However, the function as receptor for LGALS9 has been challenged (PubMed:23555261). Also reported to enhance CD8+ T-cell responses to an acute infection such as by Listeria monocytogenes (By similarity). Receptor for phosphatidylserine (PtSer); PtSer-binding is calcium-dependent. May rUniProtKB:Q8VIM0, PubMed:11823861, PubMed:14556005, PubMed:16286920, PubMed:22323453, PubMed:23555261, PubMed:24838857, PubMed:26492563, PubMed:30374066, PubMed:24825777}.

Additionnal Information

<br><br>Immunohistochemistry: use at a dilution of 1:100-1:200 on formalin-fixed, paraffin-embedded samples after heat-induced epitope retrieval at pH 9 for 10-30 minutes.

Storage Conditions

Store at 2-8°C. Do not freeze.

Specificity

Human TIM-3. Reactivity with other species has not been investigated.

Formulation

Tris buffer, pH 7.3-7.7, 1% BSA, 0.1% sodium azide.

Buffer pH

pH 7.3-7.7

Target Background

T cell immunoglobulin and mucin domain-3 (TIM-3) is a member of the TIM gene family, which includes TIM-1, TIM-3, TIM-4 in humans and Tim-1-8 in mice. TIM-3 is expressed on Th1, Th17, and CD8+ T cells as well as on dendritic cells and natural killer cells. Binding of TIM-3 and its ligands has been found to suppress Th1 and Th17 responses and induce peripheral immune tolerance, supporting an inhibitory role of TIM-3 in T cell-mediated immune responses. TIM-3 expression also characterizes exhausted T cells during chronic infection. Since administration of TIM-3 and PD-1 mAbs synergistically control tumor growth, TIM-3 is gaining importance in tumor and chronic viral infection models as a candidate for immunotherapy in conjunction with other inhibitory receptors.
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