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Human Hepcidin ELISA Kit for Sandwich ELISA - ABIN457010
Jiang, Sun, Tang, Xu, Jiao: Hepcidin expression and iron parameters change in Type 2 diabetic patients. in Diabetes research and clinical practice 2011
Show all 8 references for ABIN457010
Rat (Rattus) Hepcidin ELISA Kit for Sandwich ELISA - ABIN416434
Huang, Chuang, Yang, Huang, Wu, Chen: Cholestasis downregulate hepcidin expression through inhibiting IL-6-induced phosphorylation of signal transducer and activator of transcription 3 signaling. in Laboratory investigation; a journal of technical methods and pathology 2009
Show all 5 references for ABIN416434
Mouse (Murine) Hepcidin ELISA Kit for Sandwich ELISA - ABIN415686
Shin, Chung, Joe, Pae, Chang, Cho, Ryter, Chung: Pretreatment with CO-releasing molecules suppresses hepcidin expression during inflammation and endoplasmic reticulum stress through inhibition of the STAT3 and CREBH pathways. in Blood 2012
Show all 2 references for ABIN415686
Pig (Porcine) Hepcidin ELISA Kit for Competition ELISA - ABIN2761945
Pu, Guo, Liu, Xiong, Wang, Du: Iron Supplementation Attenuates the Inflammatory Status of Anemic Piglets by Regulating Hepcidin. in Biological trace element research 2015
The data also show that the antibacterial activity of hepcidin-2 depends upon the disulfide bridges.
data support an alternative mechanism for hepcidin regulation during zebrafish embryonic development, which is independent of hemojuvelin (show HFE2 ELISA Kits).
Hepcidin expression is regulated by a transferrin-a (show Tf ELISA Kits)-dependent pathway in the zebrafish embryo.
The data of in vitro and in vivo research evidenced on involvement of Hepc in formation of breast cancer cells malignant phenotype and their resistance to doxorubicin.
Hepcidin was a more influential determinant of iron stores than blood loss and dietary factors combined, and increased hepcidin diminished the positive association between iron intake and iron stores.
These results suggest that the ingestion of a high (compared to low) CHO (show COL11A1 ELISA Kits) diet over a seven-day training period is ineffective in attenuating post-exercise IL-6 (show IL6 ELISA Kits) and hepcidin responses. Such results may be due to the modest training load, the increased protein intake in the low-CHO (show COL11A1 ELISA Kits) trial, and a 48 h recovery period prior to sample collection on day 7, allowing a full recovery of muscle glycogen (show GYS1 ELISA Kits) status between exercise sessi
The NGAL (show LCN2 ELISA Kits)/hepcidin ratio is more strongly associated with severe of acute kidney injury than the single biomarkers alone
serum NGAL (show LCN2 ELISA Kits) and hepcidin levels might be valuable for the evaluation of inflammation in chronic kidney disease, not related through iron metabolism
study shows that patients with CRA had high expression of BMP6 (show BMP6 ELISA Kits) and hepcidin and low expression of s-HJV (show HFE2 ELISA Kits). BMP6 (show BMP6 ELISA Kits) was found to be negatively correlated with s-HJV (show HFE2 ELISA Kits); both regulate hepcidin expression and play important roles in the development of anemia.
REVIEW: outline of recent discoveries in understanding how hepcidin and its receptor ferroportin (show SLC40A1 ELISA Kits) are regulated, how they contribute to anemia of inflammation, and how this knowledge may help guide new diagnostic and therapeutic strategies for this disease
During pregnancy, in women with sufficient iron supplementation, hepcidin is low and does not reflect iron status. During delivery and the postpartum period, hepcidin functions as a marker of inflammation.
TGF-beta1 (show TGFB1 ELISA Kits) may contribute to hepcidin synthesis during iron overload.
Low hepcidin levels are associated with type 2 diabetes mellitus.
Increased hepcidin in transferrin (show Tf ELISA Kits)-treated thalassemic mice correlates with increased liver BMP2 (show BMP2 ELISA Kits) expression and decreased hepatocyte ERK (show EPHB2 ELISA Kits) activation.
The combined data presented here highlighted a crucial role of ERFE in regulating hepcidin expression and systematic iron homeostasis under phenylhydrazine-induced hemolytic anemia.
Results indicate that an efficient induction of hepcidin expression by hemojuvelin (HJV (show HFE2 ELISA Kits)) requires its interaction with neogenin (show NEO1 ELISA Kits).
The results suggest that physiologic hepcidin levels are insufficient to alter Fpn levels within the retinal pigment epithelium and Muller cells, but may limit iron transport into the retina from vascular endothelial cells.
In TNF (show TNF ELISA Kits)(DeltaARE/+) and IL-10 (show IL10 ELISA Kits)(-/-)-mice hepatic hepcidin expression and protein content was significantly lower than in corresponding wild-types.
In Angiotensin II treated mice, duodenal divalent metal transporter-1 (show SLC11A2 ELISA Kits) and ferroportin (show SLC40A1 ELISA Kits) expression levels were increased and hepatic hepcidin mRNA expression and serum hepcidin concentration were reduced.
results clarify how commensal bacteria affect hepcidin expression and reveal a novel connection between IL-1beta and activation of BMP signaling.
Activation of TLR4 (show TLR4 ELISA Kits) signaling and NF-small ka, CyrillicB are involved in the suppression of hepcidin gene transcription by alcohol in the presence of inflammation in the liver.
Study describes extensive blood vessel damage in Alzheimer's disease brain and a reduction in hepcidin and ferroportin (show SLC40A1 ELISA Kits) levels
Hepatic hepcidin plays an important role in sepsis through regulation of iron metabolism
this study demonstrates that urine hepcidin-25 concentrations strongly correlate with hepatic hepcidin mRNA abundance, plasma hepcidin-25 levels, iron transferrin (show Tf ELISA Kits) saturation and non-heme liver iron levels.
Data suugest that hepcidin might had antiinflammatory function and is a candidate regulator of the cross-talk between iron regulation and inflammation.
report the full-length cDNA sequences of porcine hepcidin and liver-expressed antimicrobial peptide-2 (LEAP-2 (show LEAP2 ELISA Kits))
Hepcidin peptide is up-regulated by iron and bacterial components in the trout liver.
The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure.
hepcidin antimicrobial peptide
, antimicrobial peptide
, iron regulatory peptide
, preprohepcidin 1
, liver-expressed antimicrobial peptide 1
, putative liver tumor regressor
, hepcidin antimicrobial peptide 1
, antimicrobial peptide hepcidin
, putative hepcidin antibacterial peptide