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Product Name SLC40A1 Chinese Name The cell membrane铁TransporterFP1抗体 Alias Ferroportin 1; Ferroportin-1; FPN1; HFE4; IREG1; Iron regulated transporter 1; Iron-regulated transporter 1; MTP1; S40A1_HUMAN; SLC40A1; Solute carrier family 40 member 1; MST079; MSTP079; MTP1; SLC11A3. literatures Specific References (12) | SL4906R has been referenced in 12 publications.Research Area Tumour immunology Signal transduction transcriptional regulatory factor Immunogen Species Rabbit Clonality Polyclonal React Species Human, (predicted: Mouse, Rat, Dog, Pig, Rabbit, ) Applications WB=1:500-2000 ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.Theoretical molecular weight 63kDa Cellular localization The cell membrane Form Liquid Concentration 1mg/ml immunogen KLH conjugated synthetic peptide derived from human SLC40A1/FPN1: 331-430/571 Lsotype IgG Purification affinity purified by Protein A Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. PubMed PubMed Product Detail SLC40A1 may be involved in iron export from duodenal epithelial cells and also in transfer of iron between maternal and fetal circulation. It mediates iron efflux in the presence of a ferroxidase (hephaestin and/or ceruloplasmin). Defects in SLC40A1 are the cause of hemochromatosis type 4, an autosomal dominant iron-loading disorder characterized by early iron accumulation in reticuloendothelial cells and a marked increase in serum ferritin.
Function:
May be involved in iron export from duodenal epithelial cell and also in transfer of iron between maternal and fetal circulation. Mediates iron efflux in the presence of a ferroxidase (hephaestin and/or ceruloplasmin).
Subunit:
Belongs to the S1LC40A transporter family.
Subcellular Location:
Cell membrane. Localized to the basolateral membrane of polarized epithelial cells.
Tissue Specificity:
Expressed in placenta, intestine, muscle and spleen.
DISEASE:
Defects in SLC40A1 are the cause of hemochromatosis type 4 (HFE4) [MIM:606069]. HFE4 is an autosomal dominant iron-loading disorder characterized by early iron accumulation in reticuloendothelial cells and a marked increase in serum ferritin before elevation of the transferrin saturation.
Similarity:
Belongs to the ferroportin (FP) (TC 2.A.100) family. SLC40A subfamily.
SWISS:
Q9NP59
Gene ID:
30061
Database links:Entrez Gene: 30061 Human
Entrez Gene: 53945 Mouse
Omim: 604653 Human
SwissProt: Q9NP59 Human
SwissProt: Q9JHI9 Mouse
Unigene: 643005 Human
Unigene: 28756 Mouse
Unigene: 15324 Rat
Product Picture Sample:
Lane 1: Human Hepg2 cell lysates
Lane 2: Human K562 cell lysates
Lane 3: Human Molt-4 cell lysates
Lane 4: Human Jurkat cell lysates
Primary: Anti-SLC40A1 (SL4906R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 63 kDa
Observed band size: 60 kDa
Sample:
A673(Human) Cell Lysate at 30 ug
Primary: Anti-SLC40A1 (SL4906R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 63 kD
Observed band size: 65 kD
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