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| Catalog: | GBAFP-PGAP3-06080 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (PGAP3). 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: | PGAP3 Gene-specific Break Apart Probe is designed to detect potential PGAP3 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 | Post-GPI Attachment To Proteins 3 |
| Gene Summary [Provided by RefSeq] | This gene encodes a glycosylphosphatidylinositol (GPI)-specific phospholipase that primarily localizes to the Golgi apparatus. This ubiquitously expressed gene is predicted to encode a seven-transmembrane protein that removes unsaturated fatty acids from the sn-2 position of GPI. The remodeling of the constituent fatty acids on GPI is thought to be important for the proper association between GPI-anchored proteins and lipid rafts. The tethering of proteins to plasma membranes via posttranslational GPI-anchoring is thought to play a role in protein sorting and trafficking. Mutations in this gene cause an autosomal recessive form of neurologic hyperphosphatasia with cognitive disability (HPMRS4). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017] |
| Gene Symbol | PGAP3 |
| Location | 17q12 |
| Chromosome | Chromosome17 |
| Coordinates | This gene maps to 37827374-37844310 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-PGAP3-06080-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-PGAP3-06080-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-PGAP3-06080-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-PGAP3-06080-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-PGAP3-06080-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-PGAP3-06080-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-PGAP3-06080-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-PGAP3-06080-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-PGAP3-06080-REGR | 599nm;515nm | 580nm;491nm |
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