mProX™ Human CCR4 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- GPCR Cell Lines
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Published Data
Fig.1 CCR4 promotes the tumor growth in vivo.
Volumes of CCR4 overexpressing tumors were larger than those in wild type tumors and vector control tumors (P<0.01). All the primary tumors were evaluated by pathologic examinatio. The result showed that microvessel density was significantly increased in tumors formed by CCR4-overexpressing cells.
Ref: Li, Ji-Yu, et al. "The chemokine receptor CCR4 promotes tumor growth and lung metastasis in breast cancer." Breast cancer research and treatment 131 (2012): 837-848.
Pubmed: 21479551
DOI: 10.1007/s10549-011-1502-6
Research Highlights
Zacharias ZR, Houtman JCD. "OMIP-099: 31-color spectral flow cytometry panel to investigate the steady-state ." Cytometry. Part A : the journal of the International Society for Analytical , 2023.
The authors have developed a 31-color panel for the characterization of T cells in human peripheral blood (Table 1). The panel was optimized using cryopreserved peripheral blood mononuclear cells (PBMC) and includes markers (CD45RA, CD45RO, CCR7, CD95) for the identification of subsets (such as naive, T(EM), T(CM), T(EMRA), and T(SCM)) of CD4, CD8, and gammadelta T cells. Additionally, the panel includes markers (CD27, CD28) for differentiation status, markers (CD11a, CD49d, CD38, HLA-DR, CD56, CD39) for activation/antigen experience status, markers (PD-1, TIM-3) for co-inhibitory marker expression, and markers (CXCR3, CXCR5, CCR4, CCR6, Foxp3, CD25, CD127) for CD4 T helper subsets. This optimized panel allows for a comprehensive assessment of the steady-state phenotype of T cells in human peripheral blood.
Pubmed:
37814476
DOI:
10.1002/cyto.a.24799
Ou HL, et al. "[Hydnocarpin inhibits malignant progression of triple negative breast cancer via ." Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese , 2023.
The study aimed to investigate the effects of HC on the migration and invasion of TNBC cells (MDA-MB-231 and MDA-MB-436) through various assays. Results indicated that HC inhibited proliferation, colony formation, invasion, and EMT in TNBC cells and decreased the levels of YAP and YAP downstream targets (CTGF and Cyr61) at both protein and mRNA levels. Overexpression of YAP reversed the inhibitory effects of HC on proliferation, migration, and invasion. HC promoted YAP degradation through the proteasome pathway and increased its ubiquitination level. Further experiments revealed direct binding between HC, YAP, and CNOT4. Thus, HC inhibited TNBC progression through CNOT4-mediated degradation and ubiquitination of YAP.
Pubmed:
37802875
DOI:
10.19540/j.cnki.cjcmm.20230510.706