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Recombinant Human Hemojuvelin/HFE2 Protein (His Tag) (PKSH031623)

Recombinant Human Hemojuvelin/HFE2 Protein (His Tag) - 1
  • Recombinant Human Hemojuvelin/HFE2 Protein (His Tag) - 1
  • Recombinant Human Hemojuvelin/HFE2 Protein (His Tag) - 2
All Size Price Qty
100μg $ 680.00
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For research use only.

Synonyms HFE2A, HJV, JH, RGMC
Species Human
Expression Host Baculovirus-Insect Cells
Sequence Met 1-Ser 399
Accession Q6ZVN8-1
Calculated Molecular Weight 40 kDa
Observed Molecular Weight 20&34&44 kDa
Tag C-His
Bio-activity Not validated for activity
Form Liquid
Purity > 95 % as determined by reducing SDS-PAGE.
Endotoxin < 1.0 EU per μg of the protein as determined by the LAL method.
Storage Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
Shipping This product is provided as lyophilized powder which is shipped with ice packs.
Formulation Lyophilized from sterile PBS, 500mM NaCl, pH 7.0, 10% glycerol
Normally 5% - 8% trehalose, mannitol and 0.01% Tween 80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.
Background Hemojuvelin, also known as HFE2, is a membrane-bound and soluble protein which belongs to the repulsive guidance molecule (RGM) family. It is known that RGMs function through Neogenin, a homologue of the Netrin receptor deleted in colon cancer. In mammals, RGM family consists of three glycoproteins which have discrete expression patterns and functions (RGM-A, RGM-B, and RGM-C). Hemojuvelin is expressed in adult and fetal liver, heart, and skeletal muscle. Hemojuvelin acts as a bone morphogenetic protein (BMP) coreceptor. Enhancement of BMP signaling regulates hepcidin (HAMP) expression and iron metabolism. It plays a key role in iron metabolism. Hemojuvelin represents the cellular receptor for hepcidin. It may be a component of the signaling pathway which activates hepcidin or it may act as a modulator of hepcidin expression. Defects in hemojuvelin are the cause of hemochromatosis type 2A, also known as juvenile hemochromatosis (JH).
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