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| Catalog: | GBAFP-ACP2-00029 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (ACP2). 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: | ACP2 Gene-specific Break Apart Probe is designed to detect potential ACP2 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 | Acid Phosphatase 2, Lysosomal |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene belongs to the histidine acid phosphatase family, which hydrolyze orthophosphoric monoesters to alcohol and phosphate. This protein is localized to the lysosomal membrane, and is chemically and genetically distinct from the red cell acid phosphatase. Mice lacking this gene showed multiple defects, including bone structure alterations, lysosomal storage defects, and an increased tendency towards seizures. An enzymatically-inactive allele of this gene in mice showed severe growth retardation, hair-follicle abnormalities, and an ataxia-like phenotype. Alternatively spliced transcript variants have been found for this gene. A C-terminally extended isoform is also predicted to be produced by the use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism. [provided by RefSeq, Oct 2017] |
| Gene Symbol | ACP2 |
| Location | 11p12-p11 |
| Chromosome | Chromosome11 |
| Coordinates | This gene maps to 47260852-47270457 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-ACP2-00029-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-ACP2-00029-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-ACP2-00029-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-ACP2-00029-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-ACP2-00029-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-ACP2-00029-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-ACP2-00029-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-ACP2-00029-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-ACP2-00029-REGR | 599nm;515nm | 580nm;491nm |
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