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| Catalog: | GBAFP-COL27A1-11174 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (COL27A1). 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: | COL27A1 Gene-specific Break Apart Probe is designed to detect potential COL27A1 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 | Collagen Type XXVII Alpha 1 Chain |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the fibrillar collagen family, and plays a role during the calcification of cartilage and the transition of cartilage to bone. The encoded protein product is a preproprotein. It includes an N-terminal signal peptide, which is followed by an N-terminal propetide, mature peptide and a C-terminal propeptide. The N-terminal propeptide contains thrombospondin N-terminal-like and laminin G-like domains. The mature peptide is a major triple-helical region. The C-terminal propeptide, also known as COLFI domain, plays crucial roles in tissue growth and repair. Mutations in this gene cause Steel syndrome. Alternatively spliced transcript variants have been found, but the full-length nature of some variants has not been determined. [provided by RefSeq, Sep 2014] |
| Gene Symbol | COL27A1 |
| Location | 9q32 |
| Chromosome | Chromosome9 |
| Coordinates | This gene maps to 116918230-117072975 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-COL27A1-11174-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-COL27A1-11174-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-COL27A1-11174-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-COL27A1-11174-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-COL27A1-11174-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-COL27A1-11174-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-COL27A1-11174-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-COL27A1-11174-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-COL27A1-11174-REGR | 599nm;515nm | 580nm;491nm |
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