跳转至内容
Merck
CN

MABC958

Anti-TIM4/TIMD-4 Antibody, clone Kat5-18

clone Kat5-18, from hamster(Armenian)

别名:

T-cell immunoglobulin and mucin domain-containing protein 4, TIMD-4, Spleen, mucin-containing, knockout of lymphotoxin protein, SMUCKLER, T-cell immunoglobulin mucin receptor 4, TIM-4, T-cell membrane protein 4, TIM4/TIMD-4

登录 查看组织和合同定价。

选择尺寸


关于此项目

UNSPSC Code:
12352203
NACRES:
NA.43
eCl@ss:
32160702
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

Anti-TIM4/TIMD-4 Antibody, clone Kat5-18, clone Kat5-18, from hamster(Armenian)

biological source

hamster (Armenian)

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

Kat5-18, monoclonal

species reactivity

mouse

technique(s)

flow cytometry: suitable
neutralization: suitable

isotype

IgG

NCBI accession no.

UniProt accession no.

shipped in

dry ice

target post-translational modification

unmodified

Quality Level

Gene Information

mouse ... Timd4(276891)

Analysis Note

Evaluated by Flow Cytometry in Ba/F3-Tim4 cells overexpressing mouse Tim4.

Flow Cytometry Analysis: 0.1 µg of this antibody detected TIM4/TIMD-4 in Ba/F3-Tim4 cells overexpressing mouse Tim4.

Application

Flow Cytometry Analysis: A representative lot detected Tim4 immunoreactivity among 61% of the resident peritoneal Tim4+ MerTK+ macrophages from C57BL/6J mice (Nishi, C., et al. (2014). Mol. Cell. Biol. 34(8):1512-1520).
Flow Cytometry Analysis: Representative lots were conjugated with biotin and detected Tim4 immunoreactivity among mouse Mac1+ peritoneal cells (Miyanishi, M., et al. (2012). Int. Immunol. 24(9):551-559; Miyanishi, M., et al. (2007). Nature. 450(7168):435-439).
Neutralizing Analysis: A representative lot blocked Tim4-mediated engulfment of apoptotic CAD-/- thymocytes by murine peritoneal macrophages in a dose-dependent manner in culture (Miyanishi, M., et al. (2007). Nature. 450(7168):435-439).
Neutralizing Analysis: A representative lot, when administered via i.v. injection, significantly suppressed the phagocytosis activity of F40/80+ macrophages in the thymus of CAD-/- mice following intraperitoneal dexamethasone injection to induce apoptosis in the thymus (Miyanishi, M., et al. (2007). Nature. 450(7168):435-439).
Research Category
Apoptosis & Cancer
Research Sub Category
Apoptosis - Additional
This Anti-TIM4/TIMD-4 Antibody, clone Kat5-18 is validated for use in Flow Cytometry and Neutralizing for the detection of TIM4/TIMD-4.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

General description

T-cell immunoglobulin and mucin domain-containing protein 4 (UniProt Q6U7R4; also known as Spleen mucin-containing knockout of lymphotoxin protein, T-cell immunoglobulin and mucin domain containing 4, T-cell immunoglobulin mucin receptor 4, T-cell membrane protein 4, TIMD-4, Smuckler) is encoded by the Timd4 (also known as B430010N18Rik, Tim4) gene (Gene ID 276891) in murine species. Phagocytes, including macrophages, target apoptotic cells for engulfment by recognizing their surface exposed phosphatidylserine (PtdSer or PS). Macrophages employ specific receptors and opsonins for PS recognition, such as Milk-fat globule epidermal growth factor 8 (MFG-E8), protein S, growth arrest-specific 6 (Gas6), and TAM family TKR (Tyro 3, Axl, and MerTK) that function as protein S and Gs6 receptors. Tim (T-cell immunoglobulin and mucin domain-containing) family proteins, stabilins, and BAI1 also directly bind PtdSer and enhance the engulfment of apoptotic cells by phagocytes. Tim4 is shown to mediate murine resident peritoneal macrophages (rpMacs) engagment of apoptotic cells, while MerTK-mediates the engulfment of tethered target cells. Tim4- or MerTK-null mutations prevent rpMac-mediated apoptotic cell engulfment. Tim4-null, but not MerTK-null, macrophages lose their ability to tether apoptotic cells. Murine Tim4 is initially produced with a signal peptide sequence (a.a. 1-22), the removal of which yields the mature Tim4 with a large extracellular region (a.a.23-279), a transmembrane domain (a.a. 280-300), and a short cytoplasmic tail (a.a. 301-343).
~37 kDa calculated

Immunogen

Epitope: Extracellular domain
Mouse peritoneal cells.

Other Notes

Concentration: Please refer to lot specific datasheet.

Physical form

Format: Purified
Protein G Purified
Purified armenian hamster monoclonal IgG antibody in PBS without preservatives.

Preparation Note

Stable for 1 year at -20°C from date of receipt.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.

未找到合适的产品?  

试试我们的产品选型工具.

存储类别

12 - Non Combustible Liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

新产品
此项目有

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

相关内容

"Mods – modifications – small alterations can have a big impact on form and function. In the motorsports world, stock vehicles are modified to enhance their performance. Modifications, or mods, to the engine, drive train, intake and exhaust components add up to provide phenomenal performance gains that can be measured as horsepower and torque increases, which yield a competitive advantage, and result in reduced run times. In biology, proteins undergo modifications that alter their function. Some proteins require the modifications in order to perform their function effectively, whether it’s a pro-protein that is cleaved to produce an active enzyme, or a protein that is phosphorylated to facilitate a signaling process. Other proteins, such as histones, undergo modifications that regulate gene expression and alter cellular function. There are several post translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination that impact protein function and activity. As a result, the analysis of proteins and their post-translational modifications are particularly important for the study of normal and disease-associated processes. New antibodies to detect phospho Histidines are now available from EMD Millipore."

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持