STC1 Blocking Peptide (C-term)
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | P52823 |
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Other Accession | P97574, O55183 |
Gene ID | 6781 |
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Other Names | Stanniocalcin-1, STC-1, STC1, STC |
Target/Specificity | The synthetic peptide sequence is selected from aa 227~242 of HUMAN STC1 |
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 | STC1 |
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Synonyms | STC |
Function | Stimulates renal phosphate reabsorption, and could therefore prevent hypercalcemia. |
Cellular Location | Secreted. |
Tissue Location | Expressed in most tissues, with the highest levels in ovary, prostate, heart, kidney and thyroid. In the kidney, expression is confined to the nephron, specifically in the distal convoluted tubule and in the collecting tubule. Not detected in the brain, liver, spleen, peripheral blood leukocytes and adrenal medulla |
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes a secreted, homodimeric glycoprotein that is expressed in a wide variety of tissues and may have autocrine or paracrine functions. The gene contains a 5' UTR rich in CAG trinucleotide repeats. The encoded protein contains 11 conserved cysteine residues and is phosphorylated by protein kinase C exclusively on its serine residues. The protein may play a role in the regulation of renal and intestinal calcium and phosphate transport, cell metabolism, or cellular calcium/phosphate homeostasis. Overexpression of human stanniocalcin 1 in mice produces high serum phosphate levels, dwarfism, and increased metabolic rate. This gene has altered expression in hepatocellular, ovarian, and breast cancers.
References
Law,A.Y., Exp. Cell Res. 314 (16), 2975-2984 (2008)
Holmes,D.I., Cell. Signal. 20 (3), 569-579 (2008)
Chang,A.C., Genomics 47 (3), 393-398 (1998)
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