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| Catalog: | GBAFP-CEP78-10953 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CEP78). 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: | CEP78 Gene-specific Break Apart Probe is designed to detect potential CEP78 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 | Centrosomal Protein 78 |
| Gene Summary [Provided by RefSeq] | This gene encodes a centrosomal protein that is both required for the regulation of centrosome-related events during the cell cycle, and required for ciliogenesis. The encoded protein has an N-terminal leucine-rich repeat (LRR) domain with six consecutive LRR repeats, and a C-terminal coiled-coil domain. It interacts with the N-terminal catalytic domain of polo-like kinase 4 (PLK4) and colocalizes with PLK4 to the distal end of the centriole. Naturally occurring mutations in this gene cause defects in primary cilia that result in retinal degeneration and sensorineural hearing loss which are associated with cone-rod degeneration disease as well as Usher syndrome. Low expression of this gene is associated with poor prognosis of colorectal cancer patients. [provided by RefSeq, Mar 2017] |
| Gene Symbol | CEP78 |
| Location | 9q21.2 |
| Chromosome | Chromosome9 |
| Coordinates | This gene maps to 80850990-80881983 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-CEP78-10953-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-CEP78-10953-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CEP78-10953-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CEP78-10953-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CEP78-10953-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-CEP78-10953-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-CEP78-10953-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-CEP78-10953-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CEP78-10953-REGR | 599nm;515nm | 580nm;491nm |
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