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| Catalog: | CNVFP-MYO15A-13676 |
| Classification: | Copy Number Variation |
| Description: | Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MYO15A). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: | MYO15A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MYO15A genes. This product achieves the purpose of detection by hybridizing with the MYO15A gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Quantity: | 20 Tests |
| Probe Kits Volume (µL): | 40 μL |
| Hybridization Solution (µL): | 200 μL |
| Turnaround Time: | 7-10 Business Days |
| Shipping Time: | 1-2 Day Expedited Shipping |
| Shipping Conditions: | -20℃ |
| Storage Conditions: | Store at -20℃ and avoid light; |
| Gene Name | Myosin XVA |
| Gene Summary [Provided by RefSeq] | This gene encodes an unconventional myosin. This protein differs from other myosins in that it has a long N-terminal extension preceding the conserved motor domain. Studies in mice suggest that this protein is necessary for actin organization in the hair cells of the cochlea. Mutations in this gene have been associated with profound, congenital, neurosensory, nonsyndromal deafness. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Read-through transcripts containing an upstream gene and this gene have been identified, but they are not thought to encode a fusion protein. Several alternatively spliced transcript variants have been described, but their full length sequences have not been determined. [provided by RefSeq, Jul 2008] |
| Gene Symbol | MYO15A |
| Location | 17p11.2 |
| Chromosome | Chromosome17 |
| Coordinates | This gene maps to 18012019-18083116 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR | CNVFP-MYO15A-13676-OR | 573nm | 548nm | |
| 2 | RE | CNVFP-MYO15A-13676-RE | 599nm | 580nm | |
| 3 | GO | CNVFP-MYO15A-13676-GO | 551nm | 525nm | |
| 4 | GR | CNVFP-MYO15A-13676-GR | 515nm | 491nm | |
| 5 | AQ | CNVFP-MYO15A-13676-AQ | 467nm | 418nm |
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