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Gene-specific Break Apart Probe-RAG2

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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 Details

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

Order Sheet

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

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