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| Catalog: | GBAFP-PCDH11X-15575 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (PCDH11X). 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: | PCDH11X Gene-specific Break Apart Probe is designed to detect potential PCDH11X 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 | Protocadherin 11 X-linked |
| Gene Summary [Provided by RefSeq] | This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing 7 cadherin repeats, a transmembrane domain and a cytoplasmic tail that differs from those of the classical cadherins. The gene is located in a major X/Y block of homology and its Y homolog, despite divergence leading to coding region changes, is the most closely related cadherin family member. The protein is thought to play a fundamental role in cell-cell recognition essential for the segmental development and function of the central nervous system. Disruption of this gene may be associated with developmental dyslexia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014] |
| Gene Symbol | PCDH11X |
| Location | Xq21.31 |
| Chromosome | ChromosomeX |
| Coordinates | This gene maps to 91089658-91878228 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-PCDH11X-15575-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-PCDH11X-15575-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-PCDH11X-15575-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-PCDH11X-15575-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-PCDH11X-15575-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-PCDH11X-15575-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-PCDH11X-15575-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-PCDH11X-15575-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-PCDH11X-15575-REGR | 599nm;515nm | 580nm;491nm |
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