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| Catalog: | GBAFP-SNRNP200-07813 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SNRNP200). 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: | SNRNP200 Gene-specific Break Apart Probe is designed to detect potential SNRNP200 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 | Small Nuclear Ribonucleoprotein U5 Subunit 200 |
| Gene Summary [Provided by RefSeq] | Pre-mRNA splicing is catalyzed by the spliceosome, a complex of specialized RNA and protein subunits that removes introns from a transcribed pre-mRNA segment. The spliceosome consists of small nuclear RNA proteins (snRNPs) U1, U2, U4, U5 and U6, together with approximately 80 conserved proteins. U5 snRNP contains nine specific proteins. This gene encodes one of the U5 snRNP-specific proteins. This protein belongs to the DEXH-box family of putative RNA helicases. It is a core component of U4/U6-U5 snRNPs and appears to catalyze an ATP-dependent unwinding of U4/U6 RNA duplices. Mutations in this gene cause autosomal-dominant retinitis pigmentosa. Alternatively spliced transcript variants encoding different isoforms have been found, but the full-length nature of these variants has not been determined. [provided by RefSeq, Mar 2010] |
| Gene Symbol | SNRNP200 |
| Location | 2q11.2 |
| Chromosome | Chromosome2 |
| Coordinates | This gene maps to 96940073-96971307 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-SNRNP200-07813-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-SNRNP200-07813-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SNRNP200-07813-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SNRNP200-07813-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SNRNP200-07813-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-SNRNP200-07813-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-SNRNP200-07813-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-SNRNP200-07813-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SNRNP200-07813-REGR | 599nm;515nm | 580nm;491nm |
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