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anti-Mouse (Murine) Amphiregulin Antibodies:
anti-Human Amphiregulin Antibodies:
anti-Rat (Rattus) Amphiregulin Antibodies:
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Human Polyclonal Amphiregulin Primary Antibody for WB - ABIN610556
Chen, Parsons, Brautigan: Tyrosine phosphorylation of protein phosphatase 2A in response to growth stimulation and v-src transformation of fibroblasts. in The Journal of biological chemistry 1994
Show all 2 references for ABIN610556
Human Polyclonal Amphiregulin Primary Antibody for IP - ABIN181313
Johnson, Saeki, Gordon, Shoyab, Salomon, Stromberg: Autocrine action of amphiregulin in a colon carcinoma cell line and immunocytochemical localization of amphiregulin in human colon. in The Journal of cell biology 1992
Show all 2 references for ABIN181313
Human Amphiregulin Primary Antibody for ELISA - ABIN638842
Oliveras-Ferraros, Cufí, Queralt, Vazquez-Martin, Martin-Castillo, de Llorens, Bosch-Barrera, Brunet, Menendez: Cross-suppression of EGFR ligands amphiregulin and epiregulin and de-repression of FGFR3 signalling contribute to cetuximab resistance in wild-type KRAS tumour cells. in British journal of cancer 2012
AREG overexpression in osteoblasts induces a transient high bone mass phenotype in the trabecular compartment of the appendicular skeleton by a growth-related, non-cell autonomous mechanism
AREG-silenced keratinocytes plays an important role in regulation cell proliferation.
Hepatic CD206 (show MRC1 Antibodies)-positive macrophages express amphiregulin to promote the immunosuppressive activity of regulatory T cells in HBV infection.
Areg may have a role in classically activated macrophages
After activation with IL-33 (show IL33 Antibodies), expression of AREG is a dominant functional signature of gut (show GUSB Antibodies)-associated IL-33 (show IL33 Antibodies)-dependent group 2 innate lymphoid cells. The frequency and number of AREG-expressing ILC2s increases following intestinal injury.
AR induces hHSC fibrogenic activity via multiple mitogenic signaling pathways, and is upregulated in murine and human NASH (show SAMSN1 Antibodies), suggesting that AR antagonists may be clinically useful anti-fibrotics in NAFLD (show TSC2 Antibodies).
hormones and/or factors in addition to E that upregulate AREG can promote mammary gland development and have the potential to affect breast cancer risk associated with pubertal mammary gland development
Our data show that AREG is essential for ultraviolet therapy-induced contact hypersensitivity suppression.
Pre-maturation with cAMP modulators in conjunction with EGF (show EGF Antibodies)-like peptides during in vitro maturation enhances mouse oocyte developmental competence.
During high-pressure ventilation, Nrf2 (show NFE2L2 Antibodies) becomes activated and induces AREG, leading to a positive feedback loop between Nrf2 (show NFE2L2 Antibodies) and AREG, which involves the p38 MAPK (show MAPK14 Antibodies) and results in the expression of cytoprotective genes.
LH and AREG decrease BNP (show BNC2 Antibodies) and CNP (show NPPC Antibodies) production in granulosa cells and down-regulate NPR2 (show NPRL2 Antibodies) expression in cumulus cells, which together decreased oocyte cGMP to levels that permit meiotic resumption.
cloning the complete coding region; comparison of endometrial amphiregulin mRNA expression in Meishan and White composite pigs
High expression of amphiregulin is associated with hepatocellular carcinoma.
Findings show the involvement of amphiregulin and semaphorin-3A (show SEMA3A Antibodies) in the improvement of skin innervations and penetration of nerve fibers into the epidermis.
Altered AREG expression induced by diverse luteinizing hormone receptor (show LHCGR Antibodies) reactivity in granulosa cells may provide a useful marker for oocyte developmental competency
Amphiregulin enhances alpha6beta1 integrin expression and cell motility in human chondrosarcoma cells through Ras/Raf (show RAF1 Antibodies)/MEK (show MAP2K1 Antibodies)/ERK (show EPHB2 Antibodies)/AP-1 (show FOSB Antibodies) pathway.
Our findings implicate amphiregulin as a critical mediator of the estrogen response in ERalpha (show ESR1 Antibodies)-positive breast cancer
Bradykinin (BK) stimulation of human airway smooth muscle cell increases amphiregulin secretion in a mechanism dependent on BK-induced COX-2 (show COX2 Antibodies) expression.
The applied drugs showed remarkable suppression of mTOR (show FRAP1 Antibodies) expression, which might delay tumor progression. Interestingly, sorafenib and sunitinib increased AREG in HNSCC 11A and 14C
Expression profiling demonstrated that AREG-activated EGFR (show EGFR Antibodies) regulates gene expression differently than EGF (show EGF Antibodies)-activated EGFR (show EGFR Antibodies)
This study shows that TGF-alpha (show TGFA Antibodies) uses common and divergent molecular mediators to regulate E-cadherin (show CDH1 Antibodies) expression and cell invasion.
Amphiregulin co-operates with bone morphogenetic protein 15 (show BMP15 Antibodies) to increase bovine oocyte developmental competence.
Data suggest that epidermal growth factor receptor (show EGFR Antibodies) B [ErbB (show EGFR Antibodies)] isoforms and their ligands (epidermal growth factor (show EGF Antibodies) [EGF (show EGF Antibodies)], amphiregulin [AREG], and neuregulin-1 (show NRG1 Antibodies) [NRG1 (show NRG1 Antibodies)]) are expressed in uteroplacental tissues in mid- and late-phases of pregnancy.
Ligand of the EGF receptor/EGFR. Autocrine growth factor as well as a mitogen for a broad range of target cells including astrocytes, Schwann cells and fibroblasts.
schwannoma-derived growth factor
, amphiregulin (schwannoma-derived growth factor)
, amphiregulin long form
, colorectum cell-derived growth factor
, Schwannoma-derived growth factor
, amphiregulin B