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| Catalog: | GBAFP-LFNG-13569 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (LFNG). 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: | LFNG Gene-specific Break Apart Probe is designed to detect potential LFNG 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 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase |
| Gene Summary [Provided by RefSeq] | This gene is a member of the fringe gene family which also includes radical and manic fringe genes. They all encode evolutionarily conserved glycosyltransferases that act in the Notch signaling pathway to define boundaries during embryonic development. While their genomic structure is distinct from other glycosyltransferases, fringe proteins have a fucose-specific beta-1,3-N-acetylglucosaminyltransferase activity that leads to elongation of O-linked fucose residues on Notch, which alters Notch signaling. This gene product is predicted to be a single-pass type II Golgi membrane protein but it may also be secreted and proteolytically processed like the related proteins in mouse and Drosophila (PMID: 9187150). Mutations in this gene have been associated with autosomal recessive spondylocostal dysostosis 3. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009] |
| Gene Symbol | LFNG |
| Location | 7p22.3 |
| Chromosome | Chromosome7 |
| Coordinates | This gene maps to 2552162-2568063 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-LFNG-13569-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-LFNG-13569-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-LFNG-13569-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-LFNG-13569-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-LFNG-13569-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-LFNG-13569-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-LFNG-13569-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-LFNG-13569-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-LFNG-13569-REGR | 599nm;515nm | 580nm;491nm |
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