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| Catalog: | GBAFP-C2-10413 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (C2). 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: | C2 Gene-specific Break Apart Probe is designed to detect potential C2 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 | Complement C2 |
| Gene Summary [Provided by RefSeq] | Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009] |
| Gene Symbol | C2 |
| Location | 6p21.33 |
| Chromosome | Chromosome6_dbb_hap3 |
| Coordinates | This gene maps to 3199308-3205449 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-C2-10413-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-C2-10413-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-C2-10413-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-C2-10413-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-C2-10413-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-C2-10413-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-C2-10413-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-C2-10413-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-C2-10413-REGR | 599nm;515nm | 580nm;491nm |
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