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| Catalog: | GBAFP-ADAMTS2-00155 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (ADAMTS2). 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: | ADAMTS2 Gene-specific Break Apart Probe is designed to detect potential ADAMTS2 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 | ADAM Metallopeptidase With Thrombospondin Type 1 Motif 2 |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016] |
| Gene Symbol | ADAMTS2 |
| Location | 5q35.3 |
| Chromosome | Chromosome5 |
| Coordinates | This gene maps to 178537851-178772431 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-ADAMTS2-00155-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-ADAMTS2-00155-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-ADAMTS2-00155-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-ADAMTS2-00155-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-ADAMTS2-00155-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-ADAMTS2-00155-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-ADAMTS2-00155-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-ADAMTS2-00155-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-ADAMTS2-00155-REGR | 599nm;515nm | 580nm;491nm |
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