CONTACT SUPPORT
Online Inquiry
| Catalog: | GBAFP-NLRP3-15000 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (NLRP3). 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: | NLRP3 Gene-specific Break Apart Probe is designed to detect potential NLRP3 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 | NLR Family Pyrin Domain Containing 3 |
| Gene Summary [Provided by RefSeq] | This gene encodes a pyrin-like protein containing a pyrin domain, a nucleotide-binding site (NBS) domain, and a leucine-rich repeat (LRR) motif. This protein interacts with the apoptosis-associated speck-like protein PYCARD/ASC, which contains a caspase recruitment domain, and is a member of the NALP3 inflammasome complex. This complex functions as an upstream activator of NF-kappaB signaling, and it plays a role in the regulation of inflammation, the immune response, and apoptosis. Mutations in this gene are associated with familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), chronic infantile neurological cutaneous and articular (CINCA) syndrome, and neonatal-onset multisystem inflammatory disease (NOMID). Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. Alternative 5' UTR structures are suggested by available data; however, insufficient evidence is available to determine if all of the represented 5' UTR splice patterns are biologically valid. [provided by RefSeq, Oct 2008] |
| Gene Symbol | NLRP3 |
| Location | 1q44 |
| Chromosome | Chromosome1 |
| Coordinates | This gene maps to 247579457-247612406 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-NLRP3-15000-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-NLRP3-15000-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-NLRP3-15000-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-NLRP3-15000-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-NLRP3-15000-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-NLRP3-15000-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-NLRP3-15000-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-NLRP3-15000-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-NLRP3-15000-REGR | 599nm;515nm | 580nm;491nm |
Other Products