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| Catalog: | GBAFP-NIPBL-15022 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (NIPBL). 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: | NIPBL Gene-specific Break Apart Probe is designed to detect potential NIPBL 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 | NIPBL, Cohesin Loading Factor |
| Gene Summary [Provided by RefSeq] | This gene encodes the homolog of the Drosophila melanogaster Nipped-B gene product and fungal Scc2-type sister chromatid cohesion proteins. The Drosophila protein facilitates enhancer-promoter communication of remote enhancers and plays a role in developmental regulation. It is also homologous to a family of chromosomal adherins with broad roles in sister chromatid cohesion, chromosome condensation, and DNA repair. The human protein has a bipartite nuclear targeting sequence and a putative HEAT repeat. Condensins, cohesins and other complexes with chromosome-related functions also contain HEAT repeats. Mutations in this gene result in Cornelia de Lange syndrome, a disorder characterized by dysmorphic facial features, growth delay, limb reduction defects, and cognitive disability. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol | NIPBL |
| Location | 5p13.2 |
| Chromosome | Chromosome5 |
| Coordinates | This gene maps to 36876860-37065921 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-NIPBL-15022-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-NIPBL-15022-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-NIPBL-15022-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-NIPBL-15022-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-NIPBL-15022-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-NIPBL-15022-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-NIPBL-15022-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-NIPBL-15022-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-NIPBL-15022-REGR | 599nm;515nm | 580nm;491nm |
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