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| Catalog: | GBAFP-FLNA-02728 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (FLNA). 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: | FLNA Gene-specific Break Apart Probe is designed to detect potential FLNA 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 | Filamin A |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is an actin-binding protein that crosslinks actin filaments and links actin filaments to membrane glycoproteins. The encoded protein is involved in remodeling the cytoskeleton to effect changes in cell shape and migration. This protein interacts with integrins, transmembrane receptor complexes, and second messengers. Defects in this gene are a cause of several syndromes, including periventricular nodular heterotopias (PVNH1, PVNH4), otopalatodigital syndromes (OPD1, OPD2), frontometaphyseal dysplasia (FMD), Melnick-Needles syndrome (MNS), and X-linked congenital idiopathic intestinal pseudoobstruction (CIIPX). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2009] |
| Gene Symbol | FLNA |
| Location | Xq28 |
| Chromosome | ChromosomeX |
| Coordinates | This gene maps to 153576899-153603006 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-FLNA-02728-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-FLNA-02728-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-FLNA-02728-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-FLNA-02728-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-FLNA-02728-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-FLNA-02728-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-FLNA-02728-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-FLNA-02728-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-FLNA-02728-REGR | 599nm;515nm | 580nm;491nm |
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