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| Catalog: | GBAFP-ERCC5-11918 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (ERCC5). Due to this design method, our probe products can detect chromosomal rearrangements, such as translocations, by FISH.The product usually consists of a reagent combination composed of a probe with a selected dye color and a hybridization reagent. |
| Application: | ERCC5 Gene-specific Break Apart Probe is designed to detect potential ERCC5 rearrangements. This probe has been confirmed on the metaphase and interphase chromosomes by FISH. We provide a variety of dye color combinations for Break Apart Probes for customers to choose from. Probe products not only provide some classic color combinations, but also provide customized probe services. |
| Quantity: | 20 Tests |
| Probe Kits Volume (µL): | 40 μL |
| Hybridization Solution (µL): | 200 μL |
| Turnaround Time: | Within 10 Business Days |
| Shipping Time: | 1-2 Day Expedited Shipping |
| Shipping Conditions: | -20℃ |
| Storage Conditions: | Store at -20℃ and avoid light; |
| Gene Name | ERCC Excision Repair 5, Endonuclease |
| Gene Summary [Provided by RefSeq] | This gene encodes a single-strand specific DNA endonuclease that makes the 3' incision in DNA excision repair following UV-induced damage. The protein may also function in other cellular processes, including RNA polymerase II transcription, and transcription-coupled DNA repair. Mutations in this gene cause xeroderma pigmentosum complementation group G (XP-G), which is also referred to as xeroderma pigmentosum VII (XP7), a skin disorder characterized by hypersensitivity to UV light and increased susceptibility for skin cancer development following UV exposure. Some patients also develop Cockayne syndrome, which is characterized by severe growth defects, cognitive disability, and cachexia. Read-through transcription exists between this gene and the neighboring upstream BIVM (basic, immunoglobulin-like variable motif containing) gene. [provided by RefSeq, Feb 2011] |
| Gene Symbol | ERCC5 |
| Location | 13q33.1 |
| Chromosome | Chromosome13 |
| Coordinates | This gene maps to 103498190-103528351 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-ERCC5-11918-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-ERCC5-11918-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-ERCC5-11918-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-ERCC5-11918-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-ERCC5-11918-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-ERCC5-11918-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-ERCC5-11918-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-ERCC5-11918-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-ERCC5-11918-REGR | 599nm;515nm | 580nm;491nm |
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