FOLR3 Antibody (N-term) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | P41439 |
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Clone Names | 100406281 |
Gene ID | 2352 |
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Other Names | Folate receptor gamma, FR-gamma, Folate receptor 3, FOLR3 |
Target/Specificity | The synthetic peptide sequence used to generate the antibody AP13617a was selected from the N-term region of FOLR3. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay. |
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 | FOLR3 |
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Function | Binds to folate and reduced folic acid derivatives and mediates delivery of 5-methyltetrahydrofolate to the interior of cells. Isoform Short does not bind folate. |
Cellular Location | Secreted. |
Tissue Location | Spleen, thymus, bone marrow, ovarian carcinoma, and uterine carcinoma |
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes a member of the folate receptor (FOLR)family, members of which have a high affinity for folic acid andfor several reduced folic acid derivatives, and mediate delivery of5-methyltetrahydrofolate to the interior of cells. This geneincludes two polymorphic variants; the shorter one has two basedeletion in the CDS, resulting in a truncated polypeptide, comparedto the longer one. Both protein products are constitutivelysecreted in hematopoietic tissues and are potential serum markerfor certain hematopoietic malignancies. The longer protein has a71% and 79% sequence homology with the FOLR1 and FOLR2 proteins,respectively.
References
O'Byrne, M.R., et al. Birth Defects Res. Part A Clin. Mol. Teratol. 88(8):689-694(2010)Jugessur, A., et al. PLoS ONE 5 (7), E11493 (2010) :Boyles, A.L., et al. Genet. Epidemiol. 33(3):247-255(2009)Franke, B., et al. Birth Defects Res. Part A Clin. Mol. Teratol. 85(3):216-226(2009)Hillman, R.T., et al. Genome Biol. 5 (2), R8 (2004) :
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