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 >  Protein>EpCAM >EPM-H5223

Human EpCAM / TROP1 Protein, His Tag

分子别名(Synonym)

EPCAM,TACSTD1,TROP1,CD326,DIAR5,EGP2,EGP314,EGP40,ESA,GA733-2,HNPCC8,HNPCC-8,KS1,4,KSA,M4S1,MIC18,MK1

表达区间及表达系统(Source)

Human EpCAM, His Tag (EPM-H5223) is expressed from human 293 cells (HEK293). It contains AA Gln 24 - Lys 265 (Accession # AAH14785.1).

Predicted N-terminus: Gln 24

Request for sequence

蛋白结构(Molecular Characterization)

EpCAM Structure

This protein carries a polyhistidine tag at the C-terminus.

The protein has a calculated MW of 28.2 kDa. The protein migrates as 31-40 kDa when calibrated against Star Ribbon Pre-stained Protein Marker under reducing (R) condition (SDS-PAGE) due to glycosylation.

内毒素(Endotoxin)

Less than 0.1 EU per μg by the LAL method.

纯度(Purity)

>95% as determined by SDS-PAGE.

制剂(Formulation)

Lyophilized from 0.22 μm filtered solution in PBS, pH7.4 with trehalose as protectant.

Contact us for customized product form or formulation.

重构方法(Reconstitution)

Please see Certificate of Analysis for specific instructions.

For best performance, we strongly recommend you to follow the reconstitution protocol provided in the CoA.

存储(Storage)

For long term storage, the product should be stored at lyophilized state at -20°C or lower.

Please avoid repeated freeze-thaw cycles.

This product is stable after storage at:

  1. -20°C to -70°C for 12 months in lyophilized state;
  2. -70°C for 3 months under sterile conditions after reconstitution.

质量管理控制体系(QMS)

  1. 质量管理体系(ISO, GMP)
  2. 质量优势
  3. 质控流程
 

电泳(SDS-PAGE)

EpCAM SDS-PAGE

Human EpCAM, His Tag on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95% (With Star Ribbon Pre-stained Protein Marker).

 

活性(Bioactivity)-ELISA

EpCAM ELISA

Immobilized Human EpCAM, His Tag (Cat. No. EPM-H5223) at 1 μg/mL (100 μL/well) can bind Anti-EpCAM Antibody, Human IgG1 with a linear range of 0.1-2 ng/mL (QC tested).

Protocol

 
评论(4)
  1. 189XXXXXXX2
  2. 0人赞
  3. 使用这个蛋白用于核酸筛选与结合。将此蛋白通过his标签固定于钴珠上,用于核酸结合验证。也使用该蛋白进行溶液结合实验及SPR验证,做得效果符合预期。
  4. >
  5. 2024-5-7
  1. 187XXXXXXX2
  2. 0人赞
  3. 使用该蛋白产品用于ELISA实验的铺板蛋白,该蛋白产品特异性好,灵敏度高,使用微量即做出良好线性的标曲,产品质量好!
  4. >
  5. 2022-11-12
  1. 199XXXXXXX5
  2. 0人赞
  3. 合作方前期提供了该货号重组蛋白进行纳米抗体筛选,效果很不错,本次回购用于抗体亲和力检测,该批次蛋白活性依然很不错,价格亲民,值得推荐。
  4. 2024-12-30
 
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背景(Background)

EpCAM is also known as CO171A, EGP, EGP40,GA7332, KSA, M4S, MIC18, MK1, TROP1, hEGP2, and is a pan-epithelial differentiation antigen that is expressed on almost all carcinomas as 17-1A(mAb) antigen. Its constitutional function is being elucidated. It is intricately linked with the Cadherin-Catenin pathway and hence the fundamental WNT pathway responsible for intracellular signaling and polarity. The epithelial cell adhesion molecule (Ep-CAM) is known to express in most epithelial malignancies and was reported as a tumor marker or a candidate of molecular targeting therapy.
Ep-CAM cross signaling with N-cadherin involves Pi3K, resulting in the abrogation of the cadherin adhesion complexes in epithelial cells was reported. And Epithelial cell adhesion molecule (Ep-CAM) recently received increased attention as a prognostic factor in breast cancer.

文献引用(Citations)

 

前沿进展

SYL3C Aptamer-DNA Tetrahedra Conjugates Enable Near-Infrared Fluorescent Imaging of Colorectal Cancer
Huang, Li, Li et al
Int J Nanomedicine (2025) 20, 3595-3606
Abstract: SYL3C is an optimized DNA aptamer with high selectivity and affinity for the epithelial cell adhesion molecule (EpCAM), an overexpressed tumor antigen in colorectal cancer (CRC). While its cellular affinity has been validated, in vivo studies are lacking.This study modifies SYL3C with the fluorescent motif Cy7 to evaluate its metabolism and diagnostic potential in EpCAM-positive HT-29 xenograft mice using near-infrared fluorescence (NIRF). We also employ DNA Tetrahedra (DTN) to load the Cy7-DTN-SYL3C probe and assess whether this strategy improves circulation and tumor uptake of SYL3C.Cy7-SYL3C is primarily metabolized by the kidneys and enables targeted imaging of HT-29 tumors, outperforming untargeted Cy7-DTN. The DTN coupling strategy prolongs SYL3C metabolism and enhances tumor probe uptake about twice higher than Cy7-SYL3C over 24 hours.This study presents preliminary evidence for the SYL3C aptamer's potential in vivo imaging of EpCAM-positive CRC. The DTN conjugation strategy may extend the aptamer's metabolic stability and improve tumor uptake, expanding its applications in CRC diagnosis and treatment.© 2025 Huang et al.
Development and application of primary rat parathyroid cells for transplantation in hypoparathyroidism
Ma, Yang, Huang et al
Gland Surg (2025) 14 (2), 139-152
Abstract: Hypoparathyroidism (HPO) is characterized by deficient secretion of parathyroid hormone (PTH), leading to hypocalcemia and disrupted calcium homeostasis. Current treatments rely on calcium and vitamin D supplementation, which do not adequately mimic physiological PTH function. Cell-based therapies offer a potential solution, but optimal culture conditions to preserve the functional properties of primary parathyroid cells remain unclear. This study aims to develop primary rat parathyroid cell cultures that maintain hormone secretion and calcium-sensing abilities and to evaluate their therapeutic potential in a rat model of HPO.An HPO model was established in rats through surgical excision of the parathyroid glands. Primary parathyroid cells were isolated from these rats and sorted by flow cytometry using epithelial cell adhesion molecule (EpCAM) and calcium-sensing receptor (CaSR) markers. Four different culture media (CM) were tested to determine optimal conditions for sustaining cell functionality. The most effective CM was supplemented with Sonic Hedgehog (Shh), Activin A, and inhibitors of epithelial-mesenchymal transition (EMT). The cultured cells were then transplanted into HPO rats, and serum calcium and PTH levels were monitored to assess therapeutic efficacy.The optimized CM successfully preserved the hormone-secreting and calcium-sensing functions of primary parathyroid cells over multiple passages. Transplanted cells in HPO rats led to a significant increase in serum calcium and PTH levels compared to untreated controls. The restoration of these levels correlated with the alleviation of hypocalcemic symptoms, indicating effective functional integration of the transplanted cells.Primary rat parathyroid cells cultured under optimized conditions retained essential functional properties and, upon transplantation, effectively restored calcium homeostasis in an HPO rat model. These results highlight the potential of using cultured primary parathyroid cells as a viable cell-based therapy for HPO, offering a promising alternative to conventional treatments.Copyright © 2025 AME Publishing Company. All rights reserved.
Facile Cascaded Negative Magnetophoresis Chip Combined with ICP-MS for Efficient Sorting and Online Detection of Circulating Tumor Cells
Fu, Chen, He et al
Anal Chem (2025)
Abstract: The isolation and detection of circulating tumor cells (CTCs) play a significant role in early cancer diagnosis and prognosis. Negative magnetophoresis sorting is a label-free method, providing easy access to enrich intact and viable CTCs, but it struggles to meet the demands of high-throughput separation and direct downstream analysis. In this work, a facile cascaded negative magnetophoresis microfluidic chip was fabricated and online coupled to inductively coupled plasma mass spectrometry (ICP-MS) for the rapid separation and detection of rare CTCs in blood samples. The chip consisted of two parts: a negative magnetophoresis sorting zone and a negative magnetophoresis phase-transfer zone. In the sorting zone, WBCs labeled with anti-CD45-magnetic beads (MBs) dispersed in biocompatible ferrofluid were removed by magnetic attractive force, while CTCs labeled with anti-EpCAM-Eu migrated into the phase-transfer zone by magnetic repulsive force; in the phase-transfer zone, due to the stable laminar flow formed by the magnetic fluid and PBS buffer, CTCs migrated into the PBS under both the magnetic repulsive force and inertial lift force and online introduced into ICP-MS for detection. This device can achieve CTC enrichment at a high throughput of 100 μL min-1 and has the capability for direct downstream analysis and recultivation (cell viability of 99.27%). The method was applied for the detection of CTCs in real clinical blood samples from 10 patients diagnosed with various cancers, and the detection rate was 100%, providing a simple and efficient approach for clinical detection of rare CTCs.
Tumor Cell-Expressed Herpesvirus Entry Mediator Regulates Proliferation and Adaptive Immunity in Ovarian Cancer
Lu, Zhang, Li et al
Immun Inflamm Dis (2025) 13 (3), e70175
Abstract: Ovarian cancer (OvCa) is a prevalent gynecological malignancy with an increasing incidence and high mortality rate. Although the role of the herpesvirus entry mediator (HVEM), encoded by the TNFRSF14 gene, is currently considered pivotal in various types of cancer, the regulation of tumor cell-expressed HVEM in OvCa remains inadequately understood.Specimens were used to detect HVEM expression via quantitative RT-PCR and flow cytometry. The proliferation of the murine OvCa cell line ID8 was determined using the Cell Counting Kit-8, colony formation, and EdU staining assays. The immune constituents within the ascites fluid and spleen of tumor-bearing mice were analyzed by flow cytometry. Bioinformatics analysis was performed to explore cytokines, chemokines, and signaling pathways regulated by HVEM, and differential expression levels were confirmed via quantitative RT-PCR and western blot analysis.Herein, we identified a significant upregulation of HVEM in OvCa tissues compared with that in benign tissues and observed dominant expression of HVEM in CD45⁻EpCAM⁺ subsets in OvCa specimens. Tumor cell-expressed HVEM was found to promote OvCa cell proliferation by partly activating spliced X-box-binding protein 1 (XBP1s)-c-Myc signaling. In mouse models, knockdown of Tnfrsf14 in ID8 cells alleviated OvCa progression and specifically affected the frequency and function of T cells in the ascites fluid and spleen. In addition, tumor cell-expressed HVEM altered chemokine expression (CXCL1/9/10/11 and CCL2/4/5) and STAT signal activation (STAT5 and STAT6) in ID8 cells.This study investigated the effects of HVEM on OvCa and validated its potential as a therapeutic marker for treating OvCa.© 2025 The Author(s). Immunity, Inflammation and Disease published by John Wiley & Sons Ltd.
Showing 1-4 of 10481 papers.
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EpCAM靶点信息
英文全称:Epithelial cell adhesion molecule
中文全称:上皮细胞粘附分子
种类:Homo sapiens
上市药物数量:0详情
临床药物数量:11详情
最高研发阶段:申请上市
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