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Human AXL Protein expressed in HEK-293 Cells - ABIN2180607
Varnum, Young, Elliott, Garcia, Bartley, Fridell, Hunt, Trail, Clogston, Toso: Axl receptor tyrosine kinase stimulated by the vitamin K-dependent protein encoded by growth-arrest-specific gene 6. in Nature 1995
Show all 4 references for ABIN2180607
Mouse (Murine) AXL Protein expressed in Human Cells - ABIN2007365
Nagata, Ohashi, Nakano, Arita, Zong, Hanafusa, Mizuno: Identification of the product of growth arrest-specific gene 6 as a common ligand for Axl, Sky, and Mer receptor tyrosine kinases. in The Journal of biological chemistry 1997
Show all 3 references for ABIN2007365
Human AXL Protein expressed in Human Cells - ABIN2002499
Braunger, Schleithoff, Schulz, Kessler, Lammers, Ullrich, Bartram, Janssen: Intracellular signaling of the Ufo/Axl receptor tyrosine kinase is mediated mainly by a multi-substrate docking-site. in Oncogene 1997
Show all 3 references for ABIN2002499
Study provides evidence that AXL and MET are associated with cell proliferation and metastasis in lung cancer, and the crosstalk between these receptors affects tumor progression.
these results confirm the correlation between AXL and PKCalpha (show PKCa Proteins), and suggest PKCalpha (show PKCa Proteins)-AXL signaling may be a treatment target, particularly in malignant cancer cells.
Authors concluded that the molecular mechanisms of AXL mediated resistance involved in the increased activity of the PI3K (show PIK3CA Proteins)/AKT (show AKT1 Proteins) and MAPK (show MAPK1 Proteins)/ERK1/2 pathways, and AXL overexpression could promote resistance, but it can be weakened when AXL expression is silenced.
The study suggests that Axl may play a role in the function of endothelial progenitor cells, thereby being involved in the pathogenesis of preeclampsia.
Data show that strong AXL expression in surgically resected that lung adenocarcinomas (LADs) was a predictor of poor prognosis.
In this paper, we review the biology of the Gas6 (show GAS6 Proteins)/Tyro3 (show TYRO3 Proteins), Axl, and MerTK (show MERTK Proteins)(collectively named TAM (show CCNA1 Proteins) system)and the current evidence supporting its potential role in the pathogenesis of multiple sclerosis .
Data show that mononuclear leu (show ADAM10 Proteins)kocytes (PBMC) AX (show ADAM17 Proteins)L receptor tyrosine kinase (Axl) is rescued by combined matrix metalloproteases ADAM10 and TACE (ADAM17) inhibition.
suggest that targeting receptor tyrosine kinase (show RET Proteins) AXL (RTK-AXL) with BMS-777607 could represent a regimen for the treatment of primary and recurrent glioblastoma multiforme (GBM).
AXL is frequently expressed in high-grade serous ovarian cancers and its expression is significantly associated to tumors displaying poor prognosis.
Data suggest that AXL receptor tyrosine kinase (Axl) may facilitate tumour progression by promoting nasopharyngeal carcinoma (NPC (show NPC1 Proteins)) cell migration and invasion.
Axl, Mertk (show MERTK Proteins) and Tyro3 (show TYRO3 Proteins) receptors are not required for Zika virus entry and infection.
Axl plays an essential role in the regulation of NK cell development as well as natural killer effector function.
Matrix metalloproteases ADAM10 (show ADAM10 Proteins) and TACE (ADAM17 (show ADAM17 Proteins)) cleave AXL receptor tyrosine kinase (Axl) in lupus-prone leukocytes.
Gas6 (show GAS6 Proteins)/Axl and Akt (show AKT1 Proteins)/FoxO1a (show FOXO1 Proteins) were involved in protective effects of testosterone on VSMCs senescence and collagen synthesis.
Axl allows specific identification of airway macrophages, and that its expression is critical for macrophage functional compartmentalization in the airspaces or lung interstitium.
results establish TAM (show CCNA1 Proteins) receptors as both controllers of microglial physiology and potential targets for therapeutic intervention in central nervous system disease
These results suggest that TAM (show CCNA1 Proteins) receptors support NSCs survival, proliferation and differentiation by regulating expression of neurotrophins, especially the nerve growth factor.
Gas6 (show GAS6 Proteins)-induced Axl signaling is a critical driver of pancreatic cancer progression.
The results indicate that Axl and Mer (show ERH Proteins) receptors cooperatively regulate the systemic immune tolerance to male germ cell antigens.
Vascular depletion of Axl reduced vein graft stiffness. Axl expression determined the STAT1 (show STAT1 Proteins)-SOCS1 (show SOCS1 Proteins) balance in vein graft intima and progression of the remodeling.
activation of receptor tyrosine kinase (show RET Proteins) Axl inhibits the osteogenic differentiation of vascular pericytes.
The protein encoded by this gene is a member of the receptor tyrosine kinase subfamily. Although it is similar to other receptor tyrosine kinases, this protein represents a unique structure of the extracellular region that juxtaposes IgL and FNIII repeats. It transduces signals from the extracellular matrix into the cytoplasm by binding growth factors like vitamin K-dependent protein growth-arrest-specific gene 6. It is involved in the stimulation of cell proliferation and can also mediate cell aggregation by homophilic binding. Alternatively spliced transcript variants encoding different isoforms have been identified.
, AXL transforming sequence/gene
, tyrosine-protein kinase receptor UFO
, adhesion-related kinase
, ufo oncogene homolog