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| Catalog: | GBAFP-TGDS-08260 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TGDS). 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: | TGDS Gene-specific Break Apart Probe is designed to detect potential TGDS 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 | TDP-glucose 4,6-dehydratase |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is a member of the short-chain dehydrogenases/reductases (SDR) superfamily, and is thought to contain a nicotinamide adenine dinucleotide (NAD) binding domain. This large SDR family of enzymes is involved in the metabolism of a variety of compounds, including prostaglandins, retinoids, lipids, steroid hormones, and xenobiotics. Mutations in this gene have been associated with Catel-Manzke syndrome, which is characterized by Pierre Robin sequence, and radial deviation of the index finger due to the presence of an accessory bone between the index finger and its proximal phalanx. Pierre Robin sequence is defined by an undersized jaw, backwards displacement of the tongue base that causes an obstruction of the airways, and can also be associated with a cleft palate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015] |
| Gene Symbol | TGDS |
| Location | 13q32.1 |
| Chromosome | Chromosome13 |
| Coordinates | This gene maps to 95226307-95248511 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-TGDS-08260-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-TGDS-08260-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-TGDS-08260-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-TGDS-08260-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-TGDS-08260-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-TGDS-08260-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-TGDS-08260-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-TGDS-08260-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-TGDS-08260-REGR | 599nm;515nm | 580nm;491nm |
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