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| Catalog: | GBAFP-TBL1X-18044 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TBL1X). 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: | TBL1X Gene-specific Break Apart Probe is designed to detect potential TBL1X 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 | Transducin Beta Like 1 X-linked |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This encoded protein is found as a subunit in corepressor SMRT (silencing mediator for retinoid and thyroid receptors) complex along with histone deacetylase 3 protein. This gene is located adjacent to the ocular albinism gene and it is thought to be involved in the pathogenesis of the ocular albinism with late-onset sensorineural deafness phenotype. Four transcript variants encoding two different isoforms have been found for this gene. This gene is highly similar to the Y chromosome TBL1Y gene. [provided by RefSeq, Nov 2008] |
| Gene Symbol | TBL1X |
| Location | Xp22.31-p22.2 |
| Chromosome | ChromosomeX |
| Coordinates | This gene maps to 9431334-9687780 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-TBL1X-18044-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-TBL1X-18044-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-TBL1X-18044-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-TBL1X-18044-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-TBL1X-18044-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-TBL1X-18044-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-TBL1X-18044-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-TBL1X-18044-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-TBL1X-18044-REGR | 599nm;515nm | 580nm;491nm |
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