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| Catalog: | GBAFP-GSC2-03155 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (GSC2). 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: | GSC2 Gene-specific Break Apart Probe is designed to detect potential GSC2 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 | Goosecoid Homeobox 2 |
| Gene Summary [Provided by RefSeq] | Goosecoidlike (GSCL), a homeodomain-containing gene, resides in the critical region for VCFS/DGS on 22q11. Velocardiofacial syndrome (VCFS) is a developmental disorder characterized by conotruncal heart defects, craniofacial anomalies, and learning disabilities. VCFS is phenotypically related to DiGeorge syndrome (DGS) and both syndromes are associated with hemizygous 22q11 deletions. Because many of the tissues and structures affected in VCFS/DGS derive from the pharyngeal arches of the developing embryo, it is believed that haploinsufficiency of a gene involved in embryonic development may be responsible for its etiology. The gene is expressed in a limited number of adult tissues, as well as in early human development. [provided by RefSeq, Jul 2008] |
| Gene Symbol | GSC2 |
| Location | 22q11.21 |
| Chromosome | Chromosome22 |
| Coordinates | This gene maps to 19136503-19137796 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-GSC2-03155-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-GSC2-03155-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-GSC2-03155-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-GSC2-03155-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-GSC2-03155-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-GSC2-03155-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-GSC2-03155-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-GSC2-03155-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-GSC2-03155-REGR | 599nm;515nm | 580nm;491nm |
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