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STEA2 Antibody (Center) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
| Primary Accession | Q8NFT2 |
|---|---|
| Other Accession | NP_001035756.1 |
| Clone Names | 91109181 |
| Gene ID | 261729 |
|---|---|
| Other Names | Metalloreductase STEAP2, 1161-, Prostate cancer-associated protein 1, Protein up-regulated in metastatic prostate cancer, PUMPCn, Six-transmembrane epithelial antigen of prostate 2, SixTransMembrane protein of prostate 1, STEAP2, PCANAP1, STAMP1 |
| Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
| Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
| Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
| Name | STEAP2 |
|---|---|
| Synonyms | PCANAP1, STAMP1 |
| Function | Integral membrane protein that functions as a NADPH-dependent ferric-chelate reductase, using NADPH from one side of the membrane to reduce a Fe(3+) chelate that is bound on the other side of the membrane (By similarity). Mediates sequential transmembrane electron transfer from NADPH to FAD and onto heme, and finally to the Fe(3+) chelate (By similarity). Can also reduce Cu(2+) to Cu(1+) (By similarity). |
| Cellular Location | Endosome membrane {ECO:0000250|UniProtKB:Q8BWB6}; Multi-pass membrane protein. Cell membrane; Multi-pass membrane protein |
| Tissue Location | Expressed at high levels in prostate and at significantly lower levels in heart, brain, kidney, pancreas, and ovary. |
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene is a member of the STEAP family and encodes amulti-pass membrane protein that localizes to the Golgi complex,the plasma membrane, and the vesicular tubular structures in thecytosol. A highly similar protein in mouse has both ferrireductaseand cupric reductase activity, and stimulates the cellular uptakeof both iron and copper in vitro. Increased transcriptionalexpression of the human gene is associated with prostate cancerprogression. Alternate transcriptional splice variants, encodingdifferent isoforms, have been characterized.
References
Vaghjiani, R.J., et al. Tissue Eng Part A 15(8):2073-2083(2009)Denoeud, F., et al. Genome Res. 17(6):746-759(2007)Ohgami, R.S., et al. Blood 108(4):1388-1394(2006)
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