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FANCG Antibody (C-term) Blocking Peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
| Primary Accession | O15287 |
|---|---|
| Clone Names | 100507236 |
| Gene ID | 2189 |
|---|---|
| Other Names | Fanconi anemia group G protein, Protein FACG, DNA repair protein XRCC9, FANCG, XRCC9 |
| 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 | FANCG |
|---|---|
| Synonyms | XRCC9 |
| Function | DNA repair protein that may operate in a postreplication repair or a cell cycle checkpoint function. May be implicated in interstrand DNA cross-link repair and in the maintenance of normal chromosome stability. Candidate tumor suppressor gene. |
| Cellular Location | Nucleus. Cytoplasm. Note=The major form is nuclear. The minor form is cytoplasmic |
| Tissue Location | Highly expressed in testis and thymus. Found in lymphoblasts |
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Provided below are standard protocols that you may find useful for product applications.
Background
The Fanconi anemia complementation group (FANC) currentlyincludes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2,FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCMand FANCN (also called PALB2). The previously defined group FANCHis the same as FANCA. Fanconi anemia is a genetically heterogeneousrecessive disorder characterized by cytogenetic instability,hypersensitivity to DNA crosslinking agents, increased chromosomalbreakage, and defective DNA repair. The members of the Fanconianemia complementation group do not share sequence similarity; theyare related by their assembly into a common nuclear proteincomplex. This gene encodes the protein for complementation group G.
References
Bailey, S.D., et al. Diabetes Care 33(10):2250-2253(2010)Wang, C., et al. Biochemistry 49(26):5560-5569(2010)Monsees, G.M., et al. Breast Cancer Res. Treat. (2010) In press :Lipkin, S.M., et al. Cancer Prev Res (Phila) 3(5):597-603(2010)Talmud, P.J., et al. Am. J. Hum. Genet. 85(5):628-642(2009)
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