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Human FGF8 ELISA Kit for Sandwich ELISA - ABIN418595
Amable, Teixeira, Carias, Granjeiro, Borojevic: Mesenchymal stromal cell proliferation, gene expression and protein production in human platelet-rich plasma-supplemented media. in PLoS ONE 2014
FGF-8 was revealed to suppress BMP-induced osteoblast differentiation through the ERK (show EPHB2 ELISA Kits) pathway and the effects were enhanced by TNF-alpha (show TNF ELISA Kits).
Fgf8 expression is required for the continued postnatal development/maturation of the Vasopressin (show AVP ELISA Kits) and CRH (show CRH ELISA Kits) neurons in the Paraventricular nucleus.
Deregulated FGF8 and Otx2 (show OTX2 ELISA Kits)/Gbx2 (show GBX2 ELISA Kits) gene expression underlies cerebellar vermis hypoplasia in mouse model of CHARGE syndrome.
Cre fate mapping in Fgf8 mutant embryos revealed novel functions of this gene in rostral patterning center progenitor development. Disruption resulted in aberrant progenitor number and distribution in the rostral telencephalon.
Tfap2a (show TFAP2A ELISA Kits)-dependent changes in mouse facial morphology result in clefting that can be ameliorated by a reduction in Fgf8 gene dosage
Results show that DLX5 (show DLX5 ELISA Kits), p63 (show CKAP4 ELISA Kits), Pin1 (show PIN1 ELISA Kits) and FGF8 participate to the same time- and location-restricted regulatory loop essential for apical ectodermal ridge stratification, hence for normal patterning and skeletal morphogenesis of the limb buds.
This study demonistrated that Fgf8- and Fgfr1 (show FGFR1 ELISA Kits)/Fgf8-deficient mice diplay increased anxiety-like behavior and reductions in specific populations of serotonergic neurons in the brain.
Scube3 may be a critical upstream regulator of fast fiber myogenesis by modulating fgf8 signaling during zebrafish embryogenesis
Retinoic acid directly represses Fgf8 through a retinoic acid response element-mediated mechanism that promotes repressive chromatin
Together our data demonstrates that Foxc1 (show FOXC1 ELISA Kits) - Fgf8 signaling regulates mammalian jaw patterning and provides a mechanistic basis for the pathogenesis of syngnathia
Regulation of neurogenesis by Fgf8a requires Cdc42 (show CDC42 ELISA Kits) signaling and a novel Cdc42 effector (show FNBP1L ELISA Kits) protein
Our results link FGF8, c-Abl (show ABL1 ELISA Kits) and p300 (show EP300 ELISA Kits) in a regulatory pathway that controls DeltaNp63alpha protein stability and transcriptional activity.
Data indicate that overexpression of fibroblast growth factor 8 (FGF8) correlates with lymph node metastasis and poor prognosis in colorectal cancer (CRC (show CALR ELISA Kits)).
FGF8 mutations (p.Gly29_Arg34dup and p.Pro26Leu) contribute to the formation of the VATER/VACTERL association.
Together, these data demonstrate that FGF (FGFR-2 (show FGFR2 ELISA Kits) and Fgf8)signaling regulates cell proliferation and cell polarity and that these cell processes contribute to facial morphogenesis.
The oncoprotein HBXIP enhances angiogenesis and growth of breast cancer through modulating FGF8 and VEGF.
genetic association study in population in Massachusetts: Data suggest that clinical features in Kallmann syndrome (KS) are associated with genetic causes: dental agenesis/digital bony abnormalities are associated with variations/mutations in FGF8.
A novel FGF8b-binding peptide (show HP ELISA Kits) with anti-tumor effect on prostate cancer.
genetic association studies in 103 patients from US and UK: Mutations in FGF8, FGFR1 (show FGFR1 ELISA Kits), or PROKR2 (show PROKR2 ELISA Kits) contributed to 7.8% of patients with combined pituitary hormone (show CGA ELISA Kits) deficiency or septo-optic dysplasia. Data suggest genetic overlap with Kallmann syndrome.
FGF8 and FGF18 (show FGF18 ELISA Kits) signal through divergent pathways in ovarian granulosa cells, despite reportedly similar receptor activation patterns.
These results suggest that polymorphisms discovered in DECR1, CBFA2T1 (show RUNX1T1 ELISA Kits), and FGF8 may play a role in the lipid metabolism pathway affecting carcass quality traits in beef cattle.
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein is known to be a factor that supports androgen and anchorage independent growth of mammary tumor cells. Overexpression of this gene has been shown to increase tumor growth and angiogensis. The adult expression of this gene is restricted to testes and ovaries. Temporal and spatial pattern of this gene expression suggests its function as an embryonic epithelial factor. Studies of the mouse and chick homologs revealed roles in midbrain and limb development, organogenesis, embryo gastrulation and left-right axis determination. The alternative splicing of this gene results in four transcript variants.
, androgen-induced growth factor
, heparin-binding growth factor 8
, fibroblast growth factor 8 (androgen-induced)
, fibroblast growth factor 8
, fibroblast growth factor-8
, fibroblast growth factor 8 (androgen-induced) isoform 1
, fibroblast growth factor 8 (androgen-induced) isoform 2
, fibroblast growth factor 8 (androgen-induced) isoform 3