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| Catalog: | GBAFP-PWRN1-16249 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (PWRN1). 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: | PWRN1 Gene-specific Break Apart Probe is designed to detect potential PWRN1 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 | Prader-Willi Region Non-protein Coding RNA 1 |
| Gene Summary [Provided by RefSeq] | This gene is located in the Prader-Willi syndrome (PWS) region of chromosome 15, which is known to undergo imprinting. The transcript is believed to be non-coding. It is bi-allelically expressed in testis and kidney, but mono-allelically expressed from the paternal allele in brain. This gene is poly-adenylated and is known to undergo alternative splicing. Transcript variants may represent part of a complex imprinting center-SNURF-SNRPN transcription unit. The contribution of this gene to the PWS phenotype is unknown, but it has been suggested that it may play a role in establishing paternal imprinting in the PWS region, perhaps by maintaining the paternal allele in an open chromatin configuration. [provided by RefSeq, Sep 2009] |
| Gene Symbol | PWRN1 |
| Location | 15q11.2 |
| Chromosome | Chromosome15 |
| Coordinates | This gene maps to 24803303-24832926 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-PWRN1-16249-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-PWRN1-16249-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-PWRN1-16249-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-PWRN1-16249-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-PWRN1-16249-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-PWRN1-16249-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-PWRN1-16249-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-PWRN1-16249-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-PWRN1-16249-REGR | 599nm;515nm | 580nm;491nm |
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