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| Catalog: | GBAFP-TSN-18391 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TSN). 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: | TSN Gene-specific Break Apart Probe is designed to detect potential TSN 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 | Translin |
| Gene Summary [Provided by RefSeq] | This gene encodes a DNA-binding protein which specifically recognizes conserved target sequences at the breakpoint junction of chromosomal translocations. Translin polypeptides form a multimeric structure that is responsible for its DNA-binding activity. Recombination-associated motifs and translin-binding sites are present at recombination hotspots and may serve as indicators of breakpoints in genes which are fused by translocations. These binding activities may play a crucial role in chromosomal translocation in lymphoid neoplasms. This protein encoded by this gene, when complexed with translin-associated protein X, also forms a Mg ion-dependent endoribonuclease that promotes RNA-induced silencing complex (RISC) activation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2012] |
| Gene Symbol | TSN |
| Location | 2q14.3 |
| Chromosome | Chromosome2 |
| Coordinates | This gene maps to 122513120-122525428 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-TSN-18391-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-TSN-18391-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-TSN-18391-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-TSN-18391-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-TSN-18391-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-TSN-18391-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-TSN-18391-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-TSN-18391-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-TSN-18391-REGR | 599nm;515nm | 580nm;491nm |
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