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| Catalog: | GBAFP-LMNA-13605 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (LMNA). 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: | LMNA Gene-specific Break Apart Probe is designed to detect potential LMNA 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 | Lamin A/C |
| Gene Summary [Provided by RefSeq] | The nuclear lamina consists of a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure and gene expression. Vertebrate lamins consist of two types, A and B. Alternative splicing results in multiple transcript variants. Mutations in this gene lead to several diseases: Emery-Dreifuss muscular dystrophy, familial partial lipodystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy, Charcot-Marie-Tooth disease, and Hutchinson-Gilford progeria syndrome. [provided by RefSeq, Apr 2012] |
| Gene Symbol | LMNA |
| Location | 1q22 |
| Chromosome | Chromosome1 |
| Coordinates | This gene maps to 156084460-156109878 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-LMNA-13605-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-LMNA-13605-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-LMNA-13605-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-LMNA-13605-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-LMNA-13605-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-LMNA-13605-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-LMNA-13605-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-LMNA-13605-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-LMNA-13605-REGR | 599nm;515nm | 580nm;491nm |
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