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Human FGF2 Kit ELISA pour Sandwich ELISA - ABIN624947
Kühn, Willenberg, Schott, Papewalis, Stumpf, Flohé, Scherbaum, Schinner: Adipocyte-secreted factors increase osteoblast proliferation and the OPG/RANKL ratio to influence osteoclast formation. dans Molecular and cellular endocrinology 2011
Show all 26 Pubmed References
Chicken FGF2 Kit ELISA pour Sandwich ELISA - ABIN414089
Zielinska, Sawosz, Grodzik, Wierzbicki, Gromadka, Hotowy, Sawosz, Lozicki, Chwalibog: Effect of heparan sulfate and gold nanoparticles on muscle development during embryogenesis. dans International journal of nanomedicine 2012
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Mouse (Murine) FGF2 Kit ELISA pour Sandwich ELISA - ABIN625113
Ozaki, Somamoto, Kawabata, Tabata: Effect of an artificial silk elastin-like protein on the migration and collagen production of mouse fibroblasts. dans Journal of biomaterials science. Polymer edition 2014
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Rat (Rattus) FGF2 Kit ELISA pour Sandwich ELISA - ABIN365551
Rodríguez-Gómez, Banegas, Wangensteen, Quesada, Jiménez, Gómez-Morales, OValle, Duarte, Vargas: Influence of thyroid state on cardiac and renal capillary density and glomerular morphology in rats. dans The Journal of endocrinology 2013
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Human FGF2 Kit ELISA pour Competition ELISA - ABIN415057
Hotowy, Sawosz, Pineda, Sawosz, Grodzik, Chwalibog: Silver nanoparticles administered to chicken affect VEGFA and FGF2 gene expression in breast muscle and heart. dans Nanoscale research letters 2012
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Rat (Rattus) FGF2 Kit ELISA pour Competition ELISA - ABIN416389
Yang, Xia, Chen, Wei, Liu, He, Li: Electrospun fibers with plasmid bFGF polyplex loadings promote skin wound healing in diabetic rats. dans Molecular pharmaceutics 2012
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Human FGF2 Kit ELISA pour Sandwich ELISA - ABIN624948
Bashkin, Doctrow, Klagsbrun, Svahn, Folkman, Vlodavsky: Basic fibroblast growth factor binds to subendothelial extracellular matrix and is released by heparitinase and heparin-like molecules. dans Biochemistry 1989
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Human FGF2 Kit ELISA pour Sandwich ELISA - ABIN365030
A Hamid, Mohamed Ali, Yusof, George: Platelet-rich plasma (PRP): an adjuvant to hasten hamstring muscle recovery. A randomized controlled trial protocol (ISCRTN66528592). dans BMC musculoskeletal disorders 2012
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Mouse (Murine) FGF2 Kit ELISA pour Sandwich ELISA - ABIN365443
Zhang, Yang, Wang, Ru, Fan: Synthesized multiple antigenic polypeptide vaccine based on B-cell epitopes of human heparanase could elicit a potent antimetastatic effect on human hepatocellular carcinoma in vivo. dans PLoS ONE 2013
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Pig (Porcine) FGF2 Kit ELISA pour Sandwich ELISA - ABIN368478
Tang, Chen, Chiang, Chen, Chang, Chen: Differentiation Effects of Platelet-Rich Plasma Concentrations on Synovial Fluid Mesenchymal Stem Cells from Pigs Cultivated in Alginate Complex Hydrogel. dans International journal of molecular sciences 2015
Thus, FGF-2 levels in hESCs culture systems can be manipulated to generate cells with longer telomere which would be advantageous in the applications of hESCs in regenerative medicine.
Low FGF2 expression is associated with cardiac ischemia and systolic dysfunction.
Mechanical strain stimulates vasculogenesis of embryonic stem cells by the intracellular messengers ROS (Montrer ROS1 Kits ELISA), NO and calcium as well as by upregulation of angiogenesis guidance molecules and the angiogenic growth factors VEGF (Montrer VEGFA Kits ELISA), FGF-2 and PDGF (Montrer PDGFA Kits ELISA)-BB.
FGFR (Montrer FGFR2 Kits ELISA) Inhibitor Ameliorates Hypophosphatemia and Impaired Engrailed-1/Wnt (Montrer WNT2 Kits ELISA) Signaling in FGF2 High Molecular Weight Isoform
data suggest that FGF2 levels are critically related to anxiety behavior and hypothalamic pituitary- adrenal axis activity, likely through modulation of hippocampal glucocorticoid receptor (Montrer NR3C1 Kits ELISA) expression, an effect that is likely receptor mediated, albeit not by FGFR1 (Montrer FGFR1 Kits ELISA), FGFR2 (Montrer FGFR2 Kits ELISA), and FGFR3 (Montrer FGFR3 Kits ELISA).
The differentiation of ERF-overexpressing trophoblast stem cell lines also suggests that ERF may have an FGF2-independent effect during the commitment towards syncytiotrophoblasts.
Novel VF-Trap fusion protein on blockage of VEGF (Montrer VEGFA Kits ELISA) and FGF-2 activity to prevent angiogenesis.
FGF2 is an extracellular inducer of COUP-TFII (Montrer NR2F2 Kits ELISA) expression and may suppress the osteogenic potential of mesenchymal cells by inducing COUP-TFII (Montrer NR2F2 Kits ELISA) expression prior to the onset of osteogenic differentiation
clearly demonstrate the different specificity of FGF12 (Montrer FGF12 Kits ELISA)-FGFR1c2 and FGF22 (Montrer FGF22 Kits ELISA)-FGFR1c2 for well defined HS structures and suggest that it is now possible to chemoenzymatically synthesize precise HS polysaccharides that can selectively mediate growth factor signaling
These results support that controlling the aberrant expression of TGF-beta1 (Montrer TGFB1 Kits ELISA) and FGF-2 via inhibition of Wnt (Montrer WNT2 Kits ELISA)/beta-catenin (Montrer CTNNB1 Kits ELISA) signaling could serve as a potential therapeutic strategy for pulmonary fibrosis.
Results uncover a novel Sdc2 (Montrer SDC2 Kits ELISA)-Tbx16-Fgf2 pathway that regulates epithelial cell morphogenesis.
Taken together, Staphylococcus aureus induces TGF-beta1 (Montrer TGFB1 Kits ELISA) and bFGF expression through the activation of AP-1 (Montrer JUN Kits ELISA) and NF-kappaB (Montrer NFKB1 Kits ELISA) in bovine mammary gland fibroblasts.
Data suggest THBS1 (thrombospondin-1 (Montrer THBS1 Kits ELISA)) expression predominates in luteal endothelial cells; THBS2 (Montrer THBS2 Kits ELISA) expression predominates in luteinized granulosa cells. Luteinizing signals down-regulate expression of THBS1 (Montrer THBS1 Kits ELISA)/THBS2 (Montrer THBS2 Kits ELISA) but up-regulate expression of FGF2.
Mixed populations of luteal cells were treated with SU1498 (VEGF receptor 2 inhibitor) or SU5402 (FGF receptor 1 inhibitor) or control on days 0-3, 3-6 or 6-9 to determine the role of FGF2 and VEGFA (Montrer VEGFA Kits ELISA) during these specific windows.
FGF2 was crucial for luteal endothelial network formation.
Associations between reproduction and milk traits, and polymorphisms at the STAT5A (Montrer STAT5A Kits ELISA) and FGF2 gene loci, were found with STAT5A (Montrer STAT5A Kits ELISA) polymorphism for age at first calving (suggestive effect; P =0.077) and lactation milk yield (significant effect; P<0.05).
FGF2 and FGF10 (Montrer FGF10 Kits ELISA) regulate migratory activity of ovine trophoblast cells through MAPK (Montrer MAPK1 Kits ELISA)-dependent pathways.
investigation of signaling mechanisms used by FGF2 to regulate interferon-tau (IFNT) production in trophoblasts: several lines of evidence suggest that FGF2 regulates IFNT production in trophoblasts by acting through protein kinase C-delta (Montrer PKCd Kits ELISA)
Alterations in the expression of VEGF-A (Montrer VEGFA Kits ELISA) and bFGF systems suggest that angiogenic factors are involved in abnormal placental development in cloned gestations, contributing to impaired fetal development and poor survival rates.
bFGF is oxidized by lysyl oxidase (Montrer LOX Kits ELISA)
vascular endothelial growth factor indirectly stimulates smooth muscle cell proliferation and migration through the modulation of basic fibroblast growth factor and transforming growth factor beta(1 (Montrer TGFB1 Kits ELISA)) released by endothelial cells
In an in vitro assay of vascular smooth muscle cells, circRNA WDR77 (Montrer WDR77 Kits ELISA) silencing significantly inhibited cell proliferation and migration. Bioinformatics methods revealed that miR (Montrer MLXIP Kits ELISA)-124 and fibroblast growth factor 2 (FGF-2) were downstream targets of circRNA WDR77 (Montrer WDR77 Kits ELISA).
FGF2 protects the tumor cells from the antiproliferative effect of Gefitinib and largely prevents reprogramming of the proteome and phosphoproteome
High FGF2 expression is associated with colon cancer metastasis.
FGF1 and 2 strongly prevent the osteogenic commitment and differentiation of hBMSCs.
These observations identify airway smooth muscle cells -derived FGF2b as a factor needed for LMC formation by CD4 (Montrer CD4 Kits ELISA) T cells, affecting intercellular communication.
Report no relationship between serum bFGF levels and ovarian cancer microvessel density and tumor bFGF expression.
High FGF2 expression is associated with ovarian cancer.
The antitumor activity of scopoletin may be due to its strong anti-angiogenic effect, which may be mediated by its effective inhibition of ERK1 (Montrer MAPK3 Kits ELISA), VEGF-A (Montrer VEGFA Kits ELISA), and FGF-2.
TGF-beta (Montrer TGFB1 Kits ELISA), bFGF and epimorphin (Montrer STX2 Kits ELISA) in the extracellular microenvironment cooperatively affect HSF (Montrer HSF1 Kits ELISA) behaviors under the control of a highly sulfated (Montrer SULF1 Kits ELISA) chondroitin sulfate
High FGF2 expression is associated with lung cancer.
Continuous passive motion can promote b-FGF expression to enhance type III collagen (Montrer COL3A1 Kits ELISA) synthesis at the tendon-bone interface in early stage of tendon-bone repair following acute rupture of supraspinatus tendon in rabbits.
Fibroblast growth factor-2 promotes in vitro heart valve interstitial cell repair through the Akt1 (Montrer AKT1 Kits ELISA) pathway.
The overlapping relationships of 3'UTR (Montrer UTS2R Kits ELISA) ends between NUDT6 (Montrer NUDT6 Kits ELISA) and FGF-2 genes, were analyzed.
FGF2 in porcine ovary may be important for the growth of more follicles due to the localisation and concentration difference between stroma and follicle tissue.
By inducing the release of an endothelial elastase, shear stress induces an integrin-dependent release of FGF-2 from endothelial cells.
qPCR analysis demonstrated an increase in FGF-2 mRNA levels beginning on day 75 and on day 114 of pregnancy.
FGF2 activates FGFR (Montrer FGFR2 Kits ELISA) which then represses the fibroblast activation of valvular interstitial cells.
FGF2 effectively blocks transforming growth factor-beta1 (TGF-beta1 (Montrer TGFB1 Kits ELISA))-mediated myofibroblast activation
upregulation of TGFalpha or FGF2 expression is not a pre-requisite for enhanced testicular growth and increased Sertoli cell proliferation that occurs subsequent to hemicastration in the neonatal boar
These results suggest that bFGF activation of neuronal FGFR1 (Montrer FGFR1 Kits ELISA) generates filopodial processes in neurons that promote nerve-muscle interaction and facilitate NMJ establishment.
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members bind heparin and possess broad mitogenic and angiogenic activities. This protein has been implicated in diverse biological processes, such as limb and nervous system development, wound healing, and tumor growth. The mRNA for this gene contains multiple polyadenylation sites, and is alternatively translated from non-AUG (CUG) and AUG initiation codons, resulting in five different isoforms with distinct properties. The CUG-initiated isoforms are localized in the nucleus and are responsible for the intracrine effect, whereas, the AUG-initiated form is mostly cytosolic and is responsible for the paracrine and autocrine effects of this FGF.
, basic fibroblast growth factor
, heparin-binding growth factor 2
, fibroblast growth factor 2
, basic fibroblast growth factor bFGF
, Basic fibroblast growth factor
, Heparin-binding growth factor 2