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| Catalog: | GBAFP-MCM3AP-04396 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (MCM3AP). 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: | MCM3AP Gene-specific Break Apart Probe is designed to detect potential MCM3AP 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 | Minichromosome Maintenance Complex Component 3 Associated Protein |
| Gene Summary [Provided by RefSeq] | The minichromosome maintenance protein 3 (MCM3) is one of the MCM proteins essential for the initiation of DNA replication. The protein encoded by this gene is a MCM3 binding protein. It was reported to have phosphorylation-dependent DNA-primase activity, which was up-regulated in antigen immunization induced germinal center. This protein was demonstrated to be an acetyltransferase that acetylates MCM3 and plays a role in DNA replication. The mutagenesis of a nuclear localization signal of MCM3 affects the binding of this protein with MCM3, suggesting that this protein may also facilitate MCM3 nuclear localization. This gene is expressed in the brain or in neuronal tissue. An allelic variant encoding amino acid Lys at 915, instead of conserved Glu, has been identified in patients with mild intellectual disability. [provided by RefSeq, Jan 2014] |
| Gene Symbol | MCM3AP |
| Location | 21q22.3 |
| Chromosome | Chromosome21 |
| Coordinates | This gene maps to 47655047-47705236 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-MCM3AP-04396-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-MCM3AP-04396-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-MCM3AP-04396-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-MCM3AP-04396-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-MCM3AP-04396-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-MCM3AP-04396-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-MCM3AP-04396-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-MCM3AP-04396-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-MCM3AP-04396-REGR | 599nm;515nm | 580nm;491nm |
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