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| Catalog: | GBAFP-TBX1-18037 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TBX1). 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: | TBX1 Gene-specific Break Apart Probe is designed to detect potential TBX1 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 | T-box 1 |
| Gene Summary [Provided by RefSeq] | This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product shares 98% amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol | TBX1 |
| Location | 22q11.21 |
| Chromosome | Chromosome22 |
| Coordinates | This gene maps to 19744225-19771112 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-TBX1-18037-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-TBX1-18037-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-TBX1-18037-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-TBX1-18037-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-TBX1-18037-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-TBX1-18037-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-TBX1-18037-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-TBX1-18037-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-TBX1-18037-REGR | 599nm;515nm | 580nm;491nm |
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