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Rat (Rattus) EGF ELISA Kit for Sandwich ELISA - ABIN1672859
Herbst: Review of epidermal growth factor receptor biology. in International journal of radiation oncology, biology, physics 2004
Show all 3 references for ABIN1672859
Human EGF ELISA Kit for Sandwich ELISA - ABIN415062
Russo: Decreased Epidermal Growth Factor (EGF) Associated with HMGB1 and Increased Hyperactivity in Children with Autism. in Biomarker insights 2013
Show all 4 references for ABIN415062
Cow (Bovine) EGF ELISA Kit for Sandwich ELISA - ABIN856999
Huang, Zhang, Li, Song, Yan, Xu, Li: Eimeria maxima microneme protein 2 delivered as DNA vaccine and recombinant protein induces immunity against experimental homogenous challenge. in Parasitology international 2015
Mouse (Murine) EGF ELISA Kit for Sandwich ELISA - ABIN424243
Huang, Yao, Xie, Fu: 3D bioprinted extracellular matrix mimics facilitate directed differentiation of epithelial progenitors for sweat gland regeneration. in Acta biomaterialia 2016
Zebrafish scube1 (show SCUBE1 ELISA Kits) (signal peptide-CUB (complement protein C1r (show C1R ELISA Kits)/C1s (show C1S ELISA Kits), Uegf, and Bmp1 (show BMP1 ELISA Kits))-EGF (epidermal growth factor) domain-containing protein 1) is involved in primitive hematopoiesis
EGF is likely a potential paracrine/juxtacrine factor from the oocytes to regulate the function of the follicle cells.
These results suggest that there is an EGF signaling network in the zebrafish ovarian follicle, and the functionality of this network is self-regulated by its own members.
Our findings indicate that epidermal growth factor, interleukin-1beta and angiotensin II receptor, type 1 may play important roles in the pathogenesis of endometriosis.
EGF/Smurf1 (show SMURF1 ELISA Kits) inhibits Wnt (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits)-induced osteogenic differentiation and that Smurf1 (show SMURF1 ELISA Kits) downregulates Wnt/b-catenin signaling by enhancing proteasomal degradation of beta-catenin (show CTNNB1 ELISA Kits).
that strong FN1 (show FN1 ELISA Kits) promoter activity drives inappropriate expression of the biologically active portion of EGF
Stimulation of bovine oviduct epithelial cell EGFR (show EGFR ELISA Kits) with EGF (human recombinant EGF) alone or with EGF in postovulatory/follicular phases (not luteal phase) up-regulates phosphorylation of MAPKs; heat blocks effects of EGF on phosphorylation of MAPKs.
Salivary secretion of EGF was diminished in Sjogren syndrome patients.
EGF-induced sodium influx regulates EGFR (show EGFR ELISA Kits) trafficking through increased microtubule acetylation.
As serum EGF levels appear to be statistically similar in oral lichen planus (OLP) and oral squamous cell carcinoma, it seems that EGF might play a role in the pathogenesis of OLP and its cancerization
EGF induces Ca(2 (show CA2 ELISA Kits)+) sensitization in vascular smooth muscle by Rho-kinase (show ROCK1 ELISA Kits)-dependent inactivation of MLCP mediated by the EGF receptor (show EGFR ELISA Kits)/MEK (show MAP2K1 ELISA Kits)/Erk1/2 (show MAPK1/3 ELISA Kits) pathway
Results indicates that EGF +61 A>G polymorphism might increase the risk of gastric cancer, especially in Asians suggesting that EGF +61 A>G polymorphism may play an important role in the development of gastric cancer. [meta-analysis]
data suggest the EGF+61 A>G polymorphism was not related with nonsyndromic oral clefts susceptibility in a Brazilian population, but supported the different genetic background between bilateral cleft lip with or without cleft palate and cleft palate only
PXR activation stimulates EGF-mediated hepatocyte proliferation in mice, at least in part, through inhibiting FOXO3 from accelerating cell-cycle progression.
Data (including data from studies in knockout mice) suggest that Epab (embryonic poly(A)-binding protein), which is oocyte specific, is required for ability of cumulus cells and granulosa cells to exhibit responsiveness to Egf/Egfr (show EGFR ELISA Kits) signaling.
modulation of EGF signaling affects in vitro expansion and differentiation of progenitors from embryonic pancreas of both mice and man.
TLR4 (show TLR4 ELISA Kits) blockade prevented TPN (show TAPBP ELISA Kits)-associated intestinal mucosa atrophy by preserving proliferation and preventing apoptosis. This is driven by a reduction in TNF-alpha (show TNF ELISA Kits) abundance and increased EGF.
EGF is required for cardiac differentiation of P19CL6 cells through interaction with GATA-4 (show GATA4 ELISA Kits) in a time- and dose-dependent manner.
These data demonstrate that Mcl-1 (show MCL1 ELISA Kits) is essential for mammopoiesis and identify EGF as a critical trigger of Mcl-1 (show MCL1 ELISA Kits) translation to ensure survival of milk-producing alveolar cells.
results indentify EGF signalling as a robust vasculogenic inductive pathway for ATMCs, leading to their transdifferentiation into functional VSMC-like cells.
MEKK1 (show MAP2K1 ELISA Kits) PHD (show PDC ELISA Kits) controls p38 (show CRK ELISA Kits) and JNK (show MAPK8 ELISA Kits) activation during TGF-beta (show TGFB1 ELISA Kits), EGF and microtubule disruption signalling, but does not affect MAPK (show MAPK1 ELISA Kits) responses to hyperosmotic stress.
VEGFR1 (show FLT1 ELISA Kits)-mediated signaling plays a critical role in gastric ulcer healing and angiogenesis through enhanced EGF expression on VEGFR1 (show FLT1 ELISA Kits)+CXCR4 (show CXCR4 ELISA Kits)+ cells
The combination of EGF-FGF2 (show FGF2 ELISA Kits) stimulates the proliferation.
10 nM/L EGF was the optimal dose for serum-free culture, which can replace traditional standard serum medium for in vitro expansion of miniature pig bone marrow-derived mesenchymal stem cells.
EGF coordinately activates multiple cell signaling pathways critical to proliferation, migration and survival of trophectoderm cells.
progesterone-induced TACE/ADAM17 (show ADAM17 ELISA Kits) leads to production of soluble EGF domain from cumulus cells, which enhances functional changes of cumulus cells and progresses meiotic maturation of oocytes
The phase-related expression of EGF and EGFR (show EGFR ELISA Kits) in the endothelium of the uterine artery and its branches suggest the modulatory effect of EGF and its receptor on the uterine artery and the region supplying these vessels.
EGF appears to sensitize epithelial cells to the detrimental effects of IFN-alpha (show IFNA ELISA Kits) but also helps to restore barrier function in the healing phase.
Data suggest that EGF expression in endometrium varies by species and parity; in Japanese Black cows, EGF expression is consistently high, while in Holstein cows, EGF expression is down-regulated in postpartum period after second calving.
Data suggest that epidermal growth factor receptor (show EGFR ELISA Kits) B [ErbB (show EGFR ELISA Kits)] isoforms and their ligands (epidermal growth factor [EGF], amphiregulin (show AREG ELISA Kits) [AREG (show AREG ELISA Kits)], and neuregulin-1 (show NRG1 ELISA Kits) [NRG1 (show NRG1 ELISA Kits)]) are expressed in uteroplacental tissues in mid- and late-phases of pregnancy.
EGF plays a role during bovine placentation.
Data suggest that epidermal growth factor (EGF) and EGF receptors are important paracrine and/or autocrine regulators of spermatogenesis in bovine.
This gene encodes a member of the epidermal growth factor superfamily. The encoded protein is synthesized as a large precursor molecule that is proteolytically cleaved to generate the 53-amino acid epidermal growth factor peptide. This protein acts a potent mitogenic factor that plays an important role in the growth, proliferation and differentiation of numerous cell types. This protein acts by binding the high affinity cell surface receptor, epidermal growth factor receptor. Defects in this gene are the cause of hypomagnesemia type 4. Dysregulation of this gene has been associated with the growth and progression of certain cancers. Alternate splicing results in multiple transcript variants.
epidermal growth factor (beta-urogastrone)
, pro-epidermal growth factor
, Pro-epidermal growth factor precursor (EGF)