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| Catalog: | GBAFP-NSMCE2-15187 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (NSMCE2). 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: | NSMCE2 Gene-specific Break Apart Probe is designed to detect potential NSMCE2 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 | NSE2/MMS21 Homolog, SMC5-SMC6 Complex SUMO Ligase |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of a family of E3 small ubiquitin-related modifier (SUMO) ligases that mediates the attachment of a SUMO protein to proteins involved in nuclear transport, transcription, chromosome segregation and DNA repair. The encoded protein is part of the structural maintenance of chromosomes (SMC) 5/6 complex which plays a key role genome maintenance, facilitating chromosome segregation and suppressing mitotic recombination. A knockout of the orthologous mouse gene is lethal prior to embryonic day 10.5. Naturally occurring mutations in this gene, that abolish the SUMO ligase activity, are associated with primordial dwarfism and extreme insulin resistance. [provided by RefSeq, Mar 2017] |
| Gene Symbol | NSMCE2 |
| Location | 8q24.13 |
| Chromosome | Chromosome8 |
| Coordinates | This gene maps to 126104082-126379367 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-NSMCE2-15187-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-NSMCE2-15187-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-NSMCE2-15187-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-NSMCE2-15187-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-NSMCE2-15187-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-NSMCE2-15187-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-NSMCE2-15187-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-NSMCE2-15187-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-NSMCE2-15187-REGR | 599nm;515nm | 580nm;491nm |
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