MAGEC2 Antibody

Shipped with Ice Packs
In Stock

Description

Characteristics of MAGEC2 Antibody

The MAGEC2 Antibody is available in two primary forms: polyclonal and monoclonal. Key specifications include:

FeaturePolyclonal (Proteintech, Cat. 10280-1-AP) Monoclonal (Cell Signaling, Cat. #20058)
TypePolyclonal rabbit IgGMonoclonal rabbit IgG (E7B8D clone)
ImmunogenMAGEC2 fusion protein Ag0418Synthetic peptide epitope mapping to MAGEC2
ApplicationsIHC, ELISAWB, IP, IHC (paraffin-embedded)
Molecular Weight41 kDa (target protein)55 kDa (target protein)
ReactivityHumanHuman
DilutionIHC: 1:500–1:2000WB: 1:1000, IP: 1:100, IHC: 1:4000–1:16000

Both antibodies are validated for human samples, with the polyclonal version optimized for tissue-based assays and the monoclonal version suited for biochemical techniques like immunoprecipitation.

Research Findings on MAGEC2 Antibody

The antibody has been instrumental in elucidating MAGEC2’s role in oncogenesis:

2.1. Prognostic Significance in Hepatocellular Carcinoma (HCC)

  • OS: High expression → median survival = 20.3 months (P = 0.0048).

  • RFS: High expression → median survival = 14.5 months (P = 0.036).

2.2. Mechanistic Insights

  • Tumor Growth Promotion: Knockdown of MAGEC2 via shRNA in HCC cell lines (e.g., MHCC97H) reduced xenograft tumor size by 60% compared to controls (P = 0.002) .

  • Epithelial-to-Mesenchymal Transition (EMT): MAGEC2 knockdown increased epithelial markers (E-cadherin) and decreased mesenchymal markers (N-cadherin, fibronectin), suggesting its role in promoting metastasis .

  • Protein Interactions: MAGEC2 interacts with TRIM28 (a ubiquitin ligase) and TAF9 (a transcription coactivator), stabilizing its expression and facilitating oncogenic signaling .

Clinical and Therapeutic Implications

  • Biomarker Potential: Elevated MAGEC2 expression has been linked to aggressive phenotypes in breast, lung, and melanoma cancers, making it a candidate for diagnostic panels .

  • Immunotherapy Target: As a CTA, MAGEC2 is under investigation for vaccine development and adoptive T-cell therapies. Early-phase trials (e.g., MAGE-C2 peptide vaccines) have shown safety and immune responses in cancer patients .

Limitations of Current Research

  • Heterogeneity in Expression: Regional and racial differences in MAGEC2 expression (higher in East Asian HCC cohorts) necessitate diverse patient sampling in trials .

  • Mechanistic Gaps: The exact signaling pathways downstream of MAGEC2 (e.g., Cyclin E regulation, apoptosis inhibition) remain understudied .

Product Specs

Buffer
PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. Store at -20°C. Avoid freeze/thaw cycles.
Lead Time
Typically, we can ship your order within 1-3 business days of receiving it. Delivery times may vary depending on the purchase method and location. For specific delivery information, please consult your local distributors.
Synonyms
Cancer testis antigen 10 antibody; Cancer/testis antigen 10 antibody; CT10 antibody; HCA587 antibody; Hepatocellular cancer antigen 587 antibody; Hepatocellular carcinoma associated antigen 587 antibody; Hepatocellular carcinoma-associated antigen 587 antibody; MAGC2_HUMAN antibody; MAGE C2 antigen antibody; MAGE E1 antigen antibody; MAGE family member C2 antibody; MAGE-C2 antigen antibody; MAGE-E1 antigen antibody; MAGEC2 antibody; Melanoma antigen family C 2 antibody; Melanoma antigen family C2 antibody; Melanoma antigen family E 1 cancer/testis specific antibody; Melanoma associated antigen C2 antibody; Melanoma-associated antigen C2 antibody; MGC13377 antibody
Target Names
MAGEC2
Uniprot No.

Target Background

Function
MAGEC2 Antibody is proposed to enhance the ubiquitin ligase activity of RING-type zinc finger-containing E3 ubiquitin-protein ligases. In vitro, it enhances the ubiquitin ligase activity of TRIM28 and stimulates p53/TP53 ubiquitination in the presence of Ubl-conjugating enzyme UBE2H, leading to p53/TP53 degradation. MAGEC2 Antibody is proposed to act through the recruitment and/or stabilization of the Ubl-conjugating enzymes (E2) at the E3:substrate complex.
Gene References Into Functions

MAGEC2 Antibody: Gene References and Functions

  • MAGEC2 directly binds TAF9 via its CR domain, suggesting that MAGEC2 may be involved in TAF9 binding with DNA to regulate certain gene transcription. PMID: 29257297
  • Our findings revealed a previously unrecognized regulation of STAT3 activation in tumor cells by cancer/testis antigen MAGEC2, providing a molecular mechanism for the oncogenic activity of MAGEC2 in cancer cells. PMID: 27775077
  • High MAGE-C2 expression was found in 38.18% of triple-negative breast cancer tissues and in 9.09% of adjacent tissues. High MAGE-C2 expression in TNBC patients was closely associated with tumor node metastasis and shorter survival time. PMID: 27843173
  • Our study provides a suitable cell model for exploring the biological functions of MAGEC2 in malignant cells and sheds light on the molecular pathway by which MAGEC2 promotes tumor development. PMID: 27636589
  • The expressions of MAGE-C2 mRNA and MAGE-C2 protein were closely associated with the stage and metastasis of lung cancer. PMID: 26903162
  • In gastrointestinal stromal tumors, 5/51 (10%) patients expressed MAGE-C2. High-grade GIST are more likely to express MAGE-C2. MAGE-C2 also significantly correlates with mitotic rate and tumor size. PMID: 24713551
  • Our results indicate that MAGEC2 plays a role in breast cancer metastasis through inducing epithelial-mesenchymal transition. PMID: 24687377
  • Overexpression of HCA587 resulted in a significant enhancement of LMP1-induced IL-6 production. These data indicate that HCA587 is a new negative regulator of BS69. PMID: 24866244
  • MAGE-C2 promotes growth and tumorigenicity of melanoma cells, phosphorylation of KAP1, and DNA damage repair. PMID: 23096706
  • Cytotoxic T cell clones directed against MAGE-C2 peptides recognize EB81-melanoma tumor cells treated with interferon (IFN)-gamma. PMID: 22925930
  • MAGE-C2/CT10 expression in prostate cancer correlates with the degree of malignancy and indicates a higher risk for biochemical recurrence after radical prostatectomy. PMID: 21754986
  • MAGEC2 is a sensitive and novel marker for seminoma. PMID: 21780320
  • p43-57 is the first HCA587-derived major histocompatibility complex class II-restricted epitope to fulfill all prerequisites for use as a peptide vaccine in patients with HCA587-expressing tumors. PMID: 21595801
  • HCA 587 may be a valuable target antigen for diagnosis and vaccination of hepatocellular carcinoma patients. PMID: 12920247
  • Identified two antigens encoded by the MAGE-C2 gene, which are recognized by several melanoma-specific cytolytic T lymphocyte clones isolated from a melanoma patient. Both antigens are presented by HLA-A2. PMID: 14999777
  • CT10 expression was more frequently found in squamous cell carcinoma than in adenocarcinoma. PMID: 15061963
  • Due to the expression pattern of the MAGE-C2 gene, this new antigen is strictly tumor-specific. PMID: 17096150
  • The MAGE-A3 and MAGE-C2 gene promoter regions are de-methylated in the presence of activated KIT but become methylated upon inhibition of KIT, consistent with the downregulation of mRNA and protein. PMID: 17495964
  • MAGE-C2/CT-10 is expressed in hepatocellular carcinoma. PMID: 18942708
Database Links

HGNC: 13574

OMIM: 300468

KEGG: hsa:51438

STRING: 9606.ENSP00000354660

UniGene: Hs.123536

Subcellular Location
Cytoplasm. Nucleus. Note=Nuclear in germ cells. Cytoplasmic in well-differentiated hepatocellular carcinoma, nuclear in moderately- and poorly-differentiated hepatocellular carcinoma.
Tissue Specificity
Not expressed in normal tissues, except in germ cells in the seminiferous tubules and in Purkinje cells of the cerebellum. Expressed in various tumors, including melanoma, lymphoma, as well as pancreatic cancer, mammary gland cancer, non-small cell lung c

Quick Inquiry

Personal Email Detected
Please use an institutional or corporate email address for inquiries. Personal email accounts ( such as Gmail, Yahoo, and Outlook) are not accepted. *
© Copyright 2025 TheBiotek. All Rights Reserved.