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| Catalog: | GBAFP-RBM8A-16397 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (RBM8A). 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: | RBM8A Gene-specific Break Apart Probe is designed to detect potential RBM8A 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 | RNA Binding Motif Protein 8A |
| Gene Summary [Provided by RefSeq] | This gene encodes a protein with a conserved RNA-binding motif. The protein is found predominantly in the nucleus, although it is also present in the cytoplasm. It is preferentially associated with mRNAs produced by splicing, including both nuclear mRNAs and newly exported cytoplasmic mRNAs. It is thought that the protein remains associated with spliced mRNAs as a tag to indicate where introns had been present, thus coupling pre- and post-mRNA splicing events. Previously, it was thought that two genes encode this protein, RBM8A and RBM8B; it is now thought that the RBM8B locus is a pseudogene. There are two alternate translation start codons with this gene, which result in two forms of the protein. An allele mutation and a low-frequency noncoding single-nucleotide polymorphism (SNP) in this gene cause thrombocytopenia-absent radius (TAR) syndrome. [provided by RefSeq, Jul 2013] |
| Gene Symbol | RBM8A |
| Location | 1q21.1 |
| Chromosome | Chromosome1 |
| Coordinates | This gene maps to 145507556-145513535 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-RBM8A-16397-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-RBM8A-16397-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-RBM8A-16397-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-RBM8A-16397-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-RBM8A-16397-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-RBM8A-16397-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-RBM8A-16397-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-RBM8A-16397-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-RBM8A-16397-REGR | 599nm;515nm | 580nm;491nm |
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