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| Catalog: | GBAFP-ALPL-09791 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (ALPL). 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: | ALPL Gene-specific Break Apart Probe is designed to detect potential ALPL 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 | Alkaline Phosphatase, Liver/bone/kidney |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the alkaline phosphatase family of proteins. There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This enzyme may play a role in bone mineralization. Mutations in this gene have been linked to hypophosphatasia, a disorder that is characterized by hypercalcemia and skeletal defects. [provided by RefSeq, Oct 2015] |
| Gene Symbol | ALPL |
| Location | 1p36.12 |
| Chromosome | Chromosome1 |
| Coordinates | This gene maps to 21835857-21904905 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-ALPL-09791-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-ALPL-09791-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-ALPL-09791-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-ALPL-09791-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-ALPL-09791-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-ALPL-09791-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-ALPL-09791-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-ALPL-09791-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-ALPL-09791-REGR | 599nm;515nm | 580nm;491nm |
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