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| Catalog: | GBAFP-LMOD3-04242 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (LMOD3). 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: | LMOD3 Gene-specific Break Apart Probe is designed to detect potential LMOD3 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 | Leiomodin 3 |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is a member of the leiomodin family of proteins. This protein contains three actin-binding domains, a tropomyosin domain, a leucine-rich repeat domain, and a Wiskott-Aldrich syndrome protein homology 2 domain (WH2). Localization of this protein to the pointed ends of thin filaments has been observed, and there is evidence that this protein acts as a catalyst of actin nucleation, and is important to the organization of sarcomeric thin filaments in skeletal muscles. Mutations in this gene have been associated as one cause of Nemaline myopathy, as other genes have also been linked to this disorder. Nemaline myopathy is a disorder characterized by nonprogressive generalized muscle weakness and protein inclusions (nemaline bodies) in skeletal myofibers. Patients with mutations in this gene often present with a severe congenital form of the disorder. [provided by RefSeq, Jan 2015] |
| Gene Symbol | LMOD3 |
| Location | 3p14.1 |
| Chromosome | Chromosome3 |
| Coordinates | This gene maps to 69156038-69171746 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-LMOD3-04242-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-LMOD3-04242-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-LMOD3-04242-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-LMOD3-04242-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-LMOD3-04242-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-LMOD3-04242-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-LMOD3-04242-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-LMOD3-04242-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-LMOD3-04242-REGR | 599nm;515nm | 580nm;491nm |
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