ARG62816

anti-EpCAM antibody [VU-1D9] (FITC)

anti-EpCAM antibody [VU-1D9] (FITC) for Flow cytometry and Human

Controls and Markers antibody; Epithelial Marker antibody; Circulating Tumor Cells BioMarker antibody

概述

产品描述 FITC-conjugated Mouse Monoclonal antibody [VU-1D9] recognizes CD326 / EpCAM
反应物种 Hu
应用 FACS
特异性 The clone VU-1D9 recognizes an epitope within EGF-like domain I of CD326 / EpCAM, a marker of epithelial lineages. This antibody strongly stains various normal epithelial cells and carcinomas.
宿主 Mouse
克隆 Monoclonal
克隆号 VU-1D9
同位型 IgG1
靶点名称 EpCAM
抗原 Small cell lung carcinoma cell line H69.
偶联标记 FITC
別名 MIC18; EGP; Tumor-associated calcium signal transducer 1; Epithelial glycoprotein 314; KSA; Ep-CAM; Epithelial cell surface antigen; Adenocarcinoma-associated antigen; HNPCC8; Cell surface glycoprotein Trop-1; EGP40; TACSTD1; KS1/4; hEGP314; Major gastrointestinal tumor-associated protein GA733-2; M4S1; MK-1; Epithelial glycoprotein; KS 1/4 antigen; ESA; DIAR5; EGP314; Epithelial cell adhesion molecule; EGP-2; TROP1; CD antigen CD326

应用说明

应用建议
应用 推荐稀释比
FACS20 µl / 10^6 cells
应用说明 * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

属性

形式 Liquid
纯化说明 The purified antibody is conjugated with Fluorescein isothiocyanate (FITC) under optimum conditions. The reagent is free of unconjugated FITC and adjusted for direct use. No reconstitution is necessary.
缓冲液 PBS, 15 mM Sodium azide and 0.2% (w/v) high-grade protease free BSA
抗菌剂 15 mM Sodium azide
稳定剂 0.2% (w/v) high-grade protease free BSA
存放说明 Aliquot and store in the dark at 2-8°C. Keep protected from prolonged exposure to light. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项 For laboratory research only, not for drug, diagnostic or other use.

生物信息

数据库连接

GeneID: 4072 Human EPCAM

Swiss-port # P16422 Human Epithelial cell adhesion molecule

基因名称 EPCAM
全名 epithelial cell adhesion molecule
背景介绍 EpCAM is a carcinoma-associated antigen and is a member of a family that includes at least two type I membrane proteins. This antigen is expressed on most normal epithelial cells and gastrointestinal carcinomas and functions as a homotypic calcium-independent cell adhesion molecule. The antigen is being used as a target for immunotherapy treatment of human carcinomas. Mutations in this gene result in congenital tufting enteropathy. [provided by RefSeq, Dec 2008]
生物功能 EpCAM may act as a physical homophilic interaction molecule between intestinal epithelial cells (IECs) and intraepithelial lymphocytes (IELs) at the mucosal epithelium for providing immunological barrier as a first line of defense against mucosal infection. Plays a role in embryonic stem cells proliferation and differentiation. Up-regulates the expression of FABP5, MYC and cyclins A and E. [UniProt]
研究领域 Controls and Markers antibody; Epithelial Marker antibody; Circulating Tumor Cells BioMarker antibody
预测分子量 35 kDa
翻译后修饰 Hyperglycosylated in carcinoma tissue as compared with autologous normal epithelia. Glycosylation at Asn-198 is crucial for protein stability.

检测图片 (1) Click the Picture to Zoom In

  • ARG62816 anti-EpCAM antibody [VU-1D9] (FITC) FACS image

    Flow Cytometry: Human MCF7 (red-filled) and SP2 cells (black-dashed) stained with ARG62816 anti-EpCAM antibody [VU-1D9] (FITC).

克隆号文献

Superficial scrapings from breast tumors is a source for biobanking and research purposes.

Ma R et al.
Lab Invest.,  (2014)

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Multiple breast cancer cell-lines derived from a single tumor differ in their molecular characteristics and tumorigenic potential.

FACS / Human

Mosoyan G et al.
PLoS One.,  (2013)

publication_link

 

hr_line

Differential gene expression in normal esophagus and Barrett's esophagus.

IHC / Human

Wang J et al.
J Gastroenterol.,  (2009)

publication_link

 

hr_line

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.

IHC / Human

Ligtenberg MJ et al.
Nat Genet.,  (2009)

publication_link

 

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