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The protein encoded by GDF3 is a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily. De plus, nous expédions GDF3 Kits (59) et GDF3 Protéines (22) et beaucoup plus de produits pour cette protéine.
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Human Polyclonal GDF3 Primary Antibody pour IHC (p), ELISA - ABIN542892
Caricasole, van Schaik, Zeinstra, Wierikx, van Gurp, van den Pol, Looijenga, Oosterhuis, Pera, Ward, de Bruijn, Kramer, de Jong, van den Eijnden-van Raaij: Human growth-differentiation factor 3 (hGDF3): developmental regulation in human teratocarcinoma cell lines and expression in primary testicular germ cell tumours. dans Oncogene 1998
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Human Polyclonal GDF3 Primary Antibody pour IHC (p), ELISA - ABIN542891
Ducy, Karsenty: The family of bone morphogenetic proteins. dans Kidney international 2000
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the 4 of the 5 variants in [i]GDF3[/i] gene contribute different pathogenicity in congenital scoliosis, which may provide molecular evidence for clinical genetic testing.
OCT4 plays a role as a transcriptional activator for GDF3 transcription in pluripotent human embryonic carcinoma NCCIT cells and contributes to the understanding of the molecular networks of stem cell regulators in germ cell-derived pluripotency and tumorigenesis.
The results expand the spectrum of mutations associated with CHDs and first suggest the potentially disease-related GDF3 gene variant in the pathogenesis of CHDs.
first evidence that NANOG is a transcriptional activator of the expression of the oncogenic growth factor GDF3 in embryonic carcinoma cells
GDF3 expression level was significantly down-regulated in breast cancer tissues compared to the surrounding nontumorous tissues.
the conditioned medium from CHO-GDF3 could reduce PC12 cell growth and induce cell differentiation
Growth differentiation factor 3 is induced by bone morphogenetic protein 6 (BMP-6) and BMP-7 and increases luteinizing hormone receptor messenger RNA expression in human granulosa cells.
Mutation of GDF3 causes ocular and skeletal anomalies.
Present data suggested that GDF3 might play important roles in the central nervous system (CNS), especially in cerebral cortex, hippocampus and cerebellum, and it shed new light on further research of GDF3 in the central nervous system.
GDF3 regulates both of the two major characteristics of embryonic stem cells: the ability to maintain the undifferentiated state and the ability to differentiate into the full spectrum of cell types.
GDF3 regulates adipose-tissue homeostasis and energy balance under nutrient overload in part by signaling through the ALK7 receptor
GDF3 is either a bi-functional TGF-beta ligand, or, more likely, that it is a BMP inhibitor that can artificially activate Nodal signaling under non-physiological conditions.
GDF3 positivity is helpful in the diagnosis of yolk sac tumor
Data, including data from studies using knockout mice, suggest that Gdf3-Alk7 axis between adipose tissue macrophages and adipocytes represents previously unrecognized mechanism by which insulin regulates both fat metabolism/lipolysis and adiposity. (Gdf3 = growth differentiation factor-3; Alk7 = activin receptor-like kinase-7)
This work establishes PPARgamma as a required metabolic sensor and transcriptional regulator of repair macrophages and establishes GDF3 as a secreted extrinsic effector protein acting on myoblasts and serving as an exclusively macrophage-derived regeneration factor in tissue repair
GDF3 has the ability to induce progression of CD24-inducible melanoma in mice.
Mice transduced with GDF-3 displayed profound weight gain when fed with high fat diet. The phenotypes included greatly expanded adipose tissue mass, increased body adiposity, highly hypertrophic adipocytes, hepatic steatosis, and elevated plasma leptin.
Gdf3 is expressed in the inner cell mass and epiblast, and null mutants frequently exhibit abnormal formation or positioning of the anterior visceral endoderm in pre-gastrulation development
Results suggest that GDF1 and GDF3 together represent the functional mammalian homologs of Vg1.
GDF3 deficiency selectively affects white adipose through its influence on basal metabolic rates.
Xnr1 and derriere are coexpressed in the posterior paraxial mesoderm at neurula stage, and with Coco define a posttranscriptionally regulated signaling center in the chain leading to an increased TGF-beta signal on the left side of the embryo.
The protein encoded by this gene is a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily. This group of proteins is characterized by a polybasic proteolytic processing site which is cleaved to produce a mature protein containing seven conserved cysteine residues. The members of this family are regulators of cell growth and differentiation in both embryonic and adult tissues.
, growth/differentiation factor 3
, VG-1-related protein 2
, growth factor CVg1
, derriA re
, derriere (posterior determination, TGFb family member)
, derriere (tgf-beta family member)
, derriere protein