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CD24 encodes a sialoglycoprotein that is expressed on mature granulocytes and in many B cells. Additionally we are shipping CD24 Antibodies (453) and CD24 Proteins (9) and many more products for this protein.
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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.
CD24 regulates EGFR (show EGFR ELISA Kits) signaling by inhibiting EGFR (show EGFR ELISA Kits) internalization and degradation in a RhoA (show RHOA ELISA Kits)-dependent manner in gastric cancer cells.
Suggest CD24 expression as independent prognostic factor in colorectal carcinoma.
CD44 (show CD44 ELISA Kits)(+)/CD24(-) phenotype may be an important factor for malignant relapse following surgical resection and chemotherapy in patients with invasive ductal carcinoma.
we present evidence that CD44v3 immunoexpression and CD44v3+/CD24- immunophenotypes could give prognostic information associated with unfavorable clinical outcomes.
Increased CD24 gene expression is associated with pediatric medulloblastomas.
The functional CD24 A57V and TG/del polymorphisms are associated with susceptibility to multiple autoimmune diseases. (Meta-analysis)
Basal like tumors are enriched for cancer stem cells (CSC) with CD44(+)/CD24(-/low) phenotype. CD133 can detect a different population of CSC in breast carcinoma
The CD24-positive phenotype is associated with cisplatin resistance in endometrial cancer tumor xenografts and is accompanied by high expression of ABC (show ABCB6 ELISA Kits) transporters.
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