TECK
- Known as:
- TECK
- Catalog number:
- CHM-364
- Product Quantity:
- 5µg
- Category:
- -
- Supplier:
- Prospecbio
- Gene target:
- TECK
Related genes to: TECK
- Gene:
- CCL25 NIH gene
- Name:
- C-C motif chemokine ligand 25
- Previous symbol:
- SCYA25
- Synonyms:
- TECK, Ckb15
- Chromosome:
- 19p13.2
- Locus Type:
- gene with protein product
- Date approved:
- 1997-11-14
- Date modifiied:
- 2016-03-01
Related products to: TECK
Anserine Thymus Expressed Chemokine Elisa Kit (TECK)Anserine anti - Thymus Expressed Chemokine Elisa Kit (TECK)Anti-Human TECKAnti-Human TECKAnti-Human TECKAnti-Human TECKAnti-human TECK CCL25 (MAB), Source: Monoclonal Murine, MABAnti-human TECK (CCL25), bt, Source: Polyclonal bt. Rabbit, PABAnti-human TECK (CCL25), bt, Source: Polyclonal bt. Rabbit, PABAnti-human TECK (CCL25), bt, Source: Polyclonal bt. Rabbit, PABAnti-human TECK (CCL25), Source: Polyclonal Rabbit, PABAnti-human TECK (CCL25), Source: Polyclonal Rabbit, PABAnti-human TECK (CCL25), Source: Polyclonal Rabbit, PABAnti-human TECK / CCL25 (MAB), Source: Monoclonal Murine, MABanti-TECK Related articles to: TECK
- The chemokine receptor CCR9 regulates thymus colonization by T progenitors and intestinal accumulation of TCRγδ+ intraepithelial lymphocytes (IELs). CCR9-ligand chemokine CCL25 is expressed predominantly in the thymus and the small intestine. By engineering tissue-specific CCL25-deficient mice, we demonstrate that CCL25 locally produced by thymic and intestinal epithelial cells individually supports developing T cell localization in the thymus and TCRγδ+ IEL accumulation in the small intestine, respectively. Our results also reveal that thymic epithelial CCL25 facilitates T cell positive selection in the thymic cortex. We further find that intestinal epithelial CCL25 promotes nutrient sensing in the small intestine. These results indicate that epithelial CCL25 directs thymic T cell development and intestinal homeostasis in a tissue-specific paracrine manner. - Source: PubMed
Publication date: 2026/05/12
Li JieYang Mei-TingMatsuda-Lennikov MamiKalle-Youngoue FelixUshio AyaKondo KentaGluckman MelecaBando KanaAbe TakayaTakada KensukeKelly Michael CCastro Martinez FelipeChen ZuojiaWu ChuanTakahama Yousuke - This study conducted a meta-analysis across three large European cohorts (UKBB, FinnGen, and REPAIR), including 12,660 rheumatoid arthritis (RA) cases, 2,446 radiographic axial spondyloarthritis (r-axSpA) cases, and over 530,000 shared controls. - Source: PubMed
Publication date: 2026/04/23
Cabrera-Serrano Antonio JoséCarretero-Fernández MaríaPérez-Rojo BegoñaTer Horst RobCañadas-Garre MarisaCanhão HelenaQuartuccio LucaSorensen Signe BGlintborg BenteFilipescu IleanaPérez-Pampin EvaConesa-Zamora PabloSwierkot Jerzyden Broeder Alfons Ade Vita SalvatoreBrix Petersen Eva RabingLi YangCoenen Marieke J HBogunia-Kubik KatarzynaAndersen VibekeFonseca João EuricoLund Hetland MereteLópez Nevot Miguel ÁngelLópez-Medina ClementinaReyes-Zurita Fernando JesúsNetea Mihai GEscudero AlejandroCáliz RafaelCollantes-Estévez EduardoSánchez-Maldonado José ManuelSainz Juan - Papillary thyroid cancer (PTC) is the most common thyroid malignancy and is often difficult to distinguish from benign nodules using current diagnostic tools, resulting in unnecessary surgical interventions. This study aimed to identify robust, reliable, and non-invasive circulating biomarkers capable of accurately discriminating benign from malignant PTC nodules by elucidating the relationship between thyroid tissue and circulating microRNA/cytokine profiles. - Source: PubMed
Publication date: 2026/04/27
Aytatli AbdulmelikSahin AbdulkadirBarlak NeslisahCaglar Hasan OnurGundogdu BetulTatar ArzuKaratas Omer Faruk - To identify candidate biomarkers of blood stasis syndrome (BSS) associated with coronary artery disease (CAD) and explore the underlying inflammatory mechanisms. - Source: PubMed
Hongzheng L IGuosheng LinYuxuan PengAlexey Viktorovich ChurovWenwen YangJie WangJieming L UFeifei LiaoRuotong Y UYue WeiZhiru ZhaoAimei L UPeng L IAling ShenLinzi LongHua Q UChanggeng F U - Food allergies have become an increasingly serious public health issue worldwide. Ovalbumin (OVA) is the primary egg allergen, and while it has long been linked to oral sensitization, new research about the dual allergen exposure hypothesis shows that airway allergen exposure is a contributor to food allergy pathogenesis. In this study, a murine food allergy model with airway sensitization was established. Airway OVA sensitization with oral challenge induced dose- and duration-dependent allergic phenotypes, Th2 and Th17 skewing, and mast cell and eosinophil infiltration in the lungs and intestines. The microbiota dysbiosis was manifested by reduced levels of . Further results suggest that CCL25/CCR9-mediated T cell gut-homing may be involved in the intestinal allergic reactions induced by airway sensitization with an oral challenge. These findings confirm that airway food allergen sensitization with oral challenge drives lung-gut immune communication, providing new experimental evidence for safety assessment of food proteins through nonoral sensitization routes. - Source: PubMed
Publication date: 2026/04/20
Hu WeiHao ZiwenZheng ShuangyanChen YanWu YongMeng XuanyiLi XinChen Hongbing