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| Catalog: | GBAFP-NPC1-05562 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (NPC1). 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: | NPC1 Gene-specific Break Apart Probe is designed to detect potential NPC1 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 | NPC Intracellular Cholesterol Transporter 1 |
| Gene Summary [Provided by RefSeq] | This gene encodes a large protein that resides in the limiting membrane of endosomes and lysosomes and mediates intracellular cholesterol trafficking via binding of cholesterol to its N-terminal domain. It is predicted to have a cytoplasmic C-terminus, 13 transmembrane domains, and 3 large loops in the lumen of the endosome - the last loop being at the N-terminus. This protein transports low-density lipoproteins to late endosomal/lysosomal compartments where they are hydrolized and released as free cholesterol. Defects in this gene cause Niemann-Pick type C disease, a rare autosomal recessive neurodegenerative disorder characterized by over accumulation of cholesterol and glycosphingolipids in late endosomal/lysosomal compartments.[provided by RefSeq, Aug 2009] |
| Gene Symbol | NPC1 |
| Location | 18q11.2 |
| Chromosome | Chromosome18 |
| Coordinates | This gene maps to 21111462-21166581 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-NPC1-05562-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-NPC1-05562-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-NPC1-05562-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-NPC1-05562-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-NPC1-05562-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-NPC1-05562-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-NPC1-05562-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-NPC1-05562-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-NPC1-05562-REGR | 599nm;515nm | 580nm;491nm |
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