HFE Antibody (Center)
Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| IHC-P, WB, E |
---|---|
Primary Accession | Q30201 |
Other Accession | O35799 |
Reactivity | Human |
Predicted | Rat |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 40108 Da |
Antigen Region | 122-148 aa |
Gene ID | 3077 |
---|---|
Other Names | Hereditary hemochromatosis protein, HLA-H, HFE, HLAH |
Target/Specificity | This HFE antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 122-148 amino acids from the Central region of human HFE. |
Dilution | WB~~1:1000 IHC-P~~1:50~100 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | HFE Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | HFE |
---|---|
Synonyms | HLAH |
Function | Binds to transferrin receptor (TFR) and reduces its affinity for iron-loaded transferrin. |
Cellular Location | Cell membrane; Single-pass type I membrane protein |
Tissue Location | Expressed in all tissues tested except brain. |
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Provided below are standard protocols that you may find useful for product applications.
Background
HFE is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin (beta2M). It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin. The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in its gene.
References
Valenti,L., Clin J Am Soc Nephrol 4 (8), 1331-1337 (2009)
Won,J.E., Intervirology 52 (5), 239-246 (2009)
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