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| Catalog: | GBAFP-RFXANK-16489 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (RFXANK). 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: | RFXANK Gene-specific Break Apart Probe is designed to detect potential RFXANK 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 | Regulatory Factor X Associated Ankyrin Containing Protein |
| Gene Summary [Provided by RefSeq] | Major histocompatibility (MHC) class II molecules are transmembrane proteins that have a central role in development and control of the immune system. The protein encoded by this gene, along with regulatory factor X-associated protein and regulatory factor-5, forms a complex that binds to the X box motif of certain MHC class II gene promoters and activates their transcription. Once bound to the promoter, this complex associates with the non-DNA-binding factor MHC class II transactivator, which controls the cell type specificity and inducibility of MHC class II gene expression. This protein contains ankyrin repeats involved in protein-protein interactions. Mutations in this gene have been linked to bare lymphocyte syndrome type II, complementation group B. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2013] |
| Gene Symbol | RFXANK |
| Location | 19p13.11 |
| Chromosome | Chromosome19 |
| Coordinates | This gene maps to 19303007-19312678 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-RFXANK-16489-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-RFXANK-16489-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-RFXANK-16489-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-RFXANK-16489-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-RFXANK-16489-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-RFXANK-16489-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-RFXANK-16489-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-RFXANK-16489-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-RFXANK-16489-REGR | 599nm;515nm | 580nm;491nm |
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