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Increased expression of CD24 may be associated with tumor progression and prognosis in patients with uterine cervical cancer.
High CD24 expression is associated with breast neoplasms.
The early stage of root development demonstrated higher CD24 expressing cells than later stage. In conclusion, quantity of CD24 expressing cells influenced SCAPs self-renewal and multi-lineage differentiation but did not influence on cell proliferation.
These results reveal the underlying link between the HCC (show FAM126A ELISA Kits) processes mediated by CD24. Moreover, as a clear tumor promoter, CD24 is considered a potential new target for HCC (show FAM126A ELISA Kits) treatment.
Of the 66 apocrine lesions, 62 (94 %) did not express C-KIT (show KIT ELISA Kits) compared to 4/63 (6 %) of the normal glands
In this work, we analyzed the expression of CD133, FOXP3 (show FOXP3 ELISA Kits), ABCG2 (show ABCG2 ELISA Kits) and CD24 in women affected by vulvar cancer, correlating these with common clinical prognostic factors
The P-534 site in CD24 gene affects the overall survival of gastric cancer and may serve as a prognostic marker for gastric cancer.
Discussion of the roles of CD24 including the effects of CD24 gene polymorphisms on the risk of developing autoimmune diseases (review).
our results suggest that CD24 is upregulated in cervical cancer tissues and plays its functions by affecting the MAPK (show MAPK1 ELISA Kits) signaling pathway in cervical cancer.
The frequencies of CD19 (show CD19 ELISA Kits)+CD24hiCD38hi B-regulatory lymphocyte were significantly increased in children with beta-thalassemia.
mice negative or positive for CD24 did not differ in terms of tumor initiation and burden in 3 mammary and prostate tumor models tested, except for Apc1572T/+ mice, in which lack of CD24 reduced the mammary tumor burden slightly but significantly.
Loss of CD24 in Mice Leads to Metabolic Dysfunctions and a Reduction in White Adipocyte Tissue.
CD24 controls breast cancer radiation response. Loss of CD24 expression leads to radiation resistance.
Delayed wound-healing in the absence of HSA/CD24 suggests that CD24 plays an important role in this process
Findings indicate that CD24(+) antigen cells play a role in tumor migration and metastasis and support Janus kinase 2 (show JAK2 ELISA Kits) protein (JAK2 (show JAK2 ELISA Kits)) as a therapeutic target in ovarian cancer.
CD24 is a conserved marker for tracking divergent states in both reprogramming and standard pluripotent culture.
CD24 in non-immune cells might be crucialfor the guidance and recruitment of leukocytes.
CD24 expression negatively regulates the NF-kappaB (show NFKB1 ELISA Kits) pathway following experimental traumatic brain injury.
the deletion of CD24 in an HSP-driven model of autoimmunity led to the unexpected development of regulatory T cell and MDSC populations that augmented immune tolerance.
CD24 is shown in vitro and in vivo as being an important oncogene (show RAB1A ELISA Kits) in the gut (show GUSB ELISA Kits), and one that plays a critical role in the initiation and progression of carcinogenesis.
This gene encodes a sialoglycoprotein that is expressed on mature granulocytes and in many B cells. The encoded protein is anchored via a glycosyl phosphatidylinositol (GPI) link to the cell surface.
CD24 antigen (small cell lung carcinoma cluster 4 antigen)
, signal transducer CD24
, CD24 antigen
, heat-stable antigen
, nectadrin heat stable antigen
, M1/69-J11D heat stable antigen
, X62 heat stable antigen
, cluster of differentiation 24
, heat stable antigen
, lymphocyte antigen 52