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Mouse (Murine) FGF2 Protein expressed in Escherichia coli (E. coli) - ABIN2667409
Chiou, Xu, Longaker: Mitogenic and chondrogenic effects of fibroblast growth factor-2 in adipose-derived mesenchymal cells. in Biochemical and biophysical research communications 2006
Show all 5 references for ABIN2667409
Human FGF2 Protein expressed in Escherichia coli (E. coli) - ABIN2667407
Cronauer, Schulz, Seifert, Ackermann, Burchardt: Fibroblast growth factors and their receptors in urological cancers: basic research and clinical implications. in European urology 2003
Show all 5 references for ABIN2667407
Human FGF2 Protein expressed in Escherichia coli (E. coli) - ABIN2001904
Wied?ocha, Falnes, Madshus, Sandvig, Olsnes: Dual mode of signal transduction by externally added acidic fibroblast growth factor. in Cell 1994
Show all 5 references for ABIN2001904
Mouse (Murine) FGF2 Protein expressed in Escherichia coli (E. coli) - ABIN2007208
Orpana, Salven: Angiogenic and lymphangiogenic molecules in hematological malignancies. in Leukemia & lymphoma 2002
Show all 4 references for ABIN2007208
Human FGF2 Protein expressed in Escherichia coli (E. coli) - ABIN666716
Eriksson, Cousens, Weaver, Matthews: Three-dimensional structure of human basic fibroblast growth factor. in Proceedings of the National Academy of Sciences of the United States of America 1991
Show all 2 references for ABIN666716
Human FGF2 Protein expressed in Escherichia coli (E. coli) - ABIN413246
Matsukura, Muneta, Tsuji, Miyatake, Yamada, Abula, Koga, Tomita, Sekiya: Mouse synovial mesenchymal stem cells increase in yield with knee inflammation. in Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2014
(125)I-bFGF mAb inhibits growth of experimental hepatocellular carcinomas.
In vivo, GSPP treatment (200 mg/kg/d) not only inhibited the growth of colon carcinoma, but also inhibited the tumor lymphangiogenesis. Conclusion. GSPP possesses the antitumor ability by inhibiting bFGF-inducing lymphangiogenesis in vitro and in vivo, which may further inhibit tumor lymphatic metastasis.
The present study indicates that a broad array of genes associated with functions of the cytoskeleton is significantly dysregulated in the MSC (show MSC Proteins) cortex of FGF-2 knockout mice
SCN2B (show SCN2B Proteins) could play an important role in the aging-related cognitive deterioration, which is associated with the regulations of COX5A (show COX5A Proteins) and FGF-2.
Lack of fibroblast growth factor-2 results in an increased volume of the striatal target area in mice.
Low RICTOR expression was detected in quiescent, confluent mouse aortic endothelial cells, whereas high doses of FGF2 induced high RICTOR expression that was associated with strong mTORC2 (show CRTC2 Proteins)-specific protein kinase (show CDK7 Proteins) Ca and AKT (show AKT1 Proteins) phosphorylation
Endogenous FGF2 secreted by trophoectoderm cells regulates protein expression and distribution in trophectoderm cells via FGFR2 (show FGFR2 Proteins).
IL-1beta (show IL1B Proteins) promotes FGF-2 expression in chondrocytes
Collectively, these studies show that FGF signaling up-regulates expression of alphaA-crystallin (show CRYAA Proteins) both directly and indirectly via up-regulation of c-Maf (show MAF Proteins).
FGF2 monoclonal antibody inhibited angiogenesis B16-F10 (show F10 Proteins) metastatic melanoma model.
Results uncover a novel Sdc2 (show SDC2 Proteins)-Tbx16-Fgf2 pathway that regulates epithelial cell morphogenesis.
Taken together, Staphylococcus aureus induces TGF-beta1 (show TGFB1 Proteins) and bFGF expression through the activation of AP-1 (show JUN Proteins) and NF-kappaB (show NFKB1 Proteins) in bovine mammary gland fibroblasts.
Data suggest THBS1 (thrombospondin-1 (show THBS1 Proteins)) expression predominates in luteal endothelial cells; THBS2 (show THBS2 Proteins) expression predominates in luteinized granulosa cells. Luteinizing signals down-regulate expression of THBS1 (show THBS1 Proteins)/THBS2 (show THBS2 Proteins) 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 (show VEGFA Proteins) during these specific windows.
FGF2 was crucial for luteal endothelial network formation.
Associations between reproduction and milk traits, and polymorphisms at the STAT5A (show STAT5A Proteins) and FGF2 gene loci, were found with STAT5A (show STAT5A Proteins) polymorphism for age at first calving (suggestive effect; P =0.077) and lactation milk yield (significant effect; P<0.05).
FGF2 and FGF10 (show FGF10 Proteins) regulate migratory activity of ovine trophoblast cells through MAPK (show MAPK1 Proteins)-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 (show PKCd Proteins)
Alterations in the expression of VEGF-A (show VEGFA Proteins) 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 (show LOX Proteins)
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 (show TGFB1 Proteins)) released by endothelial cells
Recombinant human basic fibroblast growth factor (rhbFGF) was used as an immunogen to produce Neutralizing Monoclonal Antibody 3B1
High FGF2 expression is associated with Prostate Cancer.
Data suggest that the resulting knock-in cells and blastocysts could be used for the production of transgenic cattle that express human fibroblast growth factor 2 (hFGF2) within the bovine beta-casein (show CSN2 Proteins) gene locus.
a decrease in FGF 2 is not accompanied by increased serum pentraxin 3 (show PTX3 Proteins) levels in patients with systemic sclerosis
bFGF Polymorphism Is Associated with Disease Progression and Response to Chemotherapy in Multiple Myeloma.
pro-angiogenic responses of TRAIL, vascular endothelial growth-factor-A (VEGF-A (show VEGFA Proteins)) and fibroblast growth-factor-2 (FGF-2) either separately (10 ng/mL) or in combination were compared, followed by the assessment of proliferation, migration and tubule formation using human microvascular endothelial-1 (HMEC-1) cells.
These results suggested that elastofibroma development depended on high expression of TGF-beta1 (show TGFB1 Proteins) and bFGF.
Study showed that both aFGF (show FGF1 Proteins) and bFGF were highly expressed in cervical cancer tissues. In tumors of higher clinical stages, the expression of these factors was further enhanced, suggesting that they play a role in facilitating cervical cancer cell proliferation.
Silk scaffolds exhibit excellent cytocompatibility for human pre-adipose cells and have application potential in tissue engineering and regenerative medicine. VEGF and FGF-2 expressed on silk fibers could have a potential positive effect on pre-adipose cells, while the effect of VEGF should be further addressed in vivo.
Study identifies 2 urinary biomarkers-bFGF and TIMP3 (show TIMP3 Proteins)-that successfully detect one of the most common pediatric brain tumors, juvenile pilocytic astrocytomas, with high accuracy
Continuous passive motion can promote b-FGF expression to enhance type III collagen (show COL3A1 Proteins) 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 (show AKT1 Proteins) pathway.
The overlapping relationships of 3'UTR ends between NUDT6 (show NUDT6 Proteins) 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 (show FGFR2 Proteins) which then represses the fibroblast activation of valvular interstitial cells.
FGF2 effectively blocks transforming growth factor-beta1 (TGF-beta1 (show TGFB1 Proteins))-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 (show FGFR1 Proteins) 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