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Hamp (GeneName), Hepcidin (ProteinName), 10706_EIAAB.
Product Name:

Mouse Hamp/ Hepcidin ELISA Kit

 
Cat.#:

E1979-1m

Brand:
EIAab®
Regulatory Status:
Alternative:

Hamp1,Hepc,Hepc1

Detection Method:
ELISA
Specificity:
Natural and recombinant mouse Hepcidin
Sample Type:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Sample Data:
Research Area:
-
Product Overview:
E1979-1m is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the A Disintegrin and Metalloprotease 30 (Hepcidin) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing Hepcidin. The ELISA analytical biochemical technique of the E1979-1m kit is based on Hepcidin antibody-Hepcidin antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect Hepcidin antigen targets in samples. The ELISA Kit is designed to detect native, recombinant, Hepcidin. Appropriate sample types may include undiluted human body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
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Mouse Hamp ELISA Kit
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Product Datasheets
Datasheet:


General Annotation


Sub Unit:
N/A


Function:
Liver-produced hormone that constitutes the main circulating regulator of iron absorption and distribution across tissues. Acts by promoting endocytosis and degradation of ferroportin, leading to the retention of iron in iron-exporting cells and decreased flow of iron into plasma. Controls the major flows of iron into plasma: absorption of dietary iron in the intestine, recycling of iron by macrophages, which phagocytose old erythrocytes and other cells, and mobilization of stored iron from hepatocytes.


Subcellular Location:
Secreted


This product has not yet been referenced specifically in any publications.
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[1].
"HAMP as a modifier gene that increases the phenotypic expression of the HFE pC282Y homozygous genotype."

[2].
"Association of hepcidin promoter c.-582 A>G variant and iron overload in thalassemia major."

[3].
"Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene."

[4].
"Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes."

[5].
"Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance."

[6].
"Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis."

[7].
"The solution structure of human hepcidin, a peptide hormone with antimicrobial activity that is involved in iron uptake and hereditary hemochromatosis."

[8].
"A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload."

[9].
"Hepcidin, a urinary antimicrobial peptide synthesized in the liver."

[10].
"LEAP-1, a novel highly disulfide-bonded human peptide, exhibits antimicrobial activity."
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