CONTACT SUPPORT
Online Inquiry
| Catalog: | GBAFP-RAG2-06657 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (RAG2). 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: | RAG2 Gene-specific Break Apart Probe is designed to detect potential RAG2 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 | Recombination Activating 2 |
| Gene Summary [Provided by RefSeq] | This gene encodes a protein that is involved in the initiation of V(D)J recombination during B and T cell development. This protein forms a complex with the product of the adjacent recombination activating gene 1, and this complex can form double-strand breaks by cleaving DNA at conserved recombination signal sequences. The recombination activating gene 1 component is thought to contain most of the catalytic activity, while the N-terminal of the recombination activating gene 2 component is thought to form a six-bladed propeller in the active core that serves as a binding scaffold for the tight association of the complex with DNA. A C-terminal plant homeodomain finger-like motif in this protein is necessary for interactions with chromatin components, specifically with histone H3 that is trimethylated at lysine 4. Mutations in this gene cause Omenn syndrome, a form of severe combined immunodeficiency associated with autoimmune-like symptoms. [provided by RefSeq, Jul 2008] |
| Gene Symbol | RAG2 |
| Location | 11p12 |
| Chromosome | Chromosome11 |
| Coordinates | This gene maps to 36613492-36619829 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-RAG2-06657-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-RAG2-06657-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-RAG2-06657-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-RAG2-06657-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-RAG2-06657-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-RAG2-06657-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-RAG2-06657-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-RAG2-06657-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-RAG2-06657-REGR | 599nm;515nm | 580nm;491nm |
Other Products