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| Catalog: | GBAFP-TNXB-08626 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TNXB). 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: | TNXB Gene-specific Break Apart Probe is designed to detect potential TNXB 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 | Tenascin XB |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol | TNXB |
| Location | 6p21.33-p21.32 |
| Chromosome | Chromosome6_cox_hap2 |
| Coordinates | This gene maps to 3479582-3547813 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-TNXB-08626-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-TNXB-08626-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-TNXB-08626-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-TNXB-08626-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-TNXB-08626-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-TNXB-08626-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-TNXB-08626-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-TNXB-08626-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-TNXB-08626-REGR | 599nm;515nm | 580nm;491nm |
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