mProX™ Human CD70 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- CD Cell Lines
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Patrick Liam (Creative Biolabs Scientific Support)
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Patrick Liam (Creative Biolabs Scientific Support)
Published Data
Fig.1 Knockdown of CD70 in lung cancer cell lines.
The assessment of protein expression of CD70, EMT-transcription factors, and effectors of apoptosis was conducted via immunoblotting in HCC44 and H23 cells, which had been transfected with siRNA targeting CD70 (siCD70) or a control siRNA (siCtrl) for a duration of 96 hours.
Ref: Ortiz-Cuaran, Sandra, et al. "Epithelial-to-mesenchymal transition promotes immune escape by inducing CD70 in non-small cell lung cancer." European Journal of Cancer 169 (2022): 106-122.
Pubmed: 35550950
DOI: 10.1016/j.ejca.2022.03.038
Research Highlights
Wu, Jinfeng. et al. "LINC00887 regulates malignant progression and T-cell chemotaxis in clear cell renal cell carcinoma by activating CD70 via recruitment of SPI1." Gene, 2023.
Several articles have mentioned the involvement of LINC00887 in various cancers such as nasopharyngeal carcinoma, lung cancer, and glioma. However, the specific mechanism by which LINC00887 contributes to the malignant progression of clear cell renal cell carcinoma (ccRCC) remains unclear. This study focuses on investigating the role of LINC00887 in ccRCC malignant progression.
Wu, Jinfeng. et al. "LINC00887 regulates malignant progression and T-cell chemotaxis in clear cell renal cell carcinoma by activating CD70 via recruitment of SPI1." Gene, 2023.
Pubmed:
37858743
DOI:
10.1016/j.gene.2023.147910
Bonvino Stafuzza, Nedenia. et al. "Weighted single-step genome-wide association study and functional enrichment analyses for gastrointestinal nematode resistance traits in Santa Ines sheep." Veterinary parasitology, 2023.
In pursuit of understanding the genetic basis of gastrointestinal nematode resistance in Santa Ines sheep, a comprehensive study was conducted. The dataset consisted of 5529 records from 1703 naturally infected animals, with 37,511 SNPs from 589 animals remaining after rigorous genomic data quality control. Utilizing a weighted single-step approach for genome-wide association analysis, the study identified 20, 22, 21, and 19 genomic regions contributing significantly to fecal egg counts (FEC), Famacha© (FAM), packed cell volume (PCV), and total plasma protein (TPP), respectively. Furthermore, within these regions, a total of 81, 122, 106, and 101 protein-coding genes were found to be associated with FEC, FAM, PCV, and TPP, respectively. Notably, these genes encompassed immune system and inflammatory response functions, including ADCY9, ADRB2, BRAF, CADM1, CCL20, CD70, CREBBP, FNBP1, HTR4, IL16, IL22, IL26, MAPK8, NDFIP1, NLRC3, PAK5, PLCB1, PLCB4, ROCK1, TEK, TNFRSF12A, and VAV1. In addition, functional enrichment analysis using the DAVID tool unveiled several significant pathways and Gene Ontology terms linked to gastrointestinal nematode resistance in Santa Ines sheep, including the chemokine signaling pathway (oas04062), cAMP signaling pathway (oas04024), cGMP-PKG signaling pathway (Oas04022), platelet activation (Oas04611), Rap1 signaling pathway (oas04015), and oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen (GO:0016705). These findings represent a valuable contribution to advancing our understanding of the genetic underpinnings of gastrointestinal nematode resistance in Santa Ines sheep.
Bonvino Stafuzza, Nedenia. et al. "Weighted single-step genome-wide association study and functional enrichment analyses for gastrointestinal nematode resistance traits in Santa Ines sheep." Veterinary parasitology, 2023.
Pubmed:
37857178
DOI:
10.1016/j.vetpar.2023.110047