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| Catalog: | GBAFP-C5-00933 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (C5). 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: | C5 Gene-specific Break Apart Probe is designed to detect potential C5 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 C5 |
| Gene Summary [Provided by RefSeq] | This gene encodes a component of the complement system, a part of the innate immune system that plays an important role in inflammation, host homeostasis, and host defense against pathogens. The encoded preproprotein is proteolytically processed to generate multiple protein products, including the C5 alpha chain, C5 beta chain, C5a anaphylatoxin and C5b. The C5 protein is comprised of the C5 alpha and beta chains, which are linked by a disulfide bridge. Cleavage of the alpha chain by a convertase enzyme results in the formation of the C5a anaphylatoxin, which possesses potent spasmogenic and chemotactic activity, and the C5b macromolecular cleavage product, a subunit of the membrane attack complex (MAC). Mutations in this gene cause complement component 5 deficiency, a disease characterized by recurrent bacterial infections. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015] |
| Gene Symbol | C5 |
| Location | 9q33.2 |
| Chromosome | Chromosome9 |
| Coordinates | This gene maps to 123714613-123812554 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-C5-00933-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-C5-00933-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-C5-00933-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-C5-00933-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-C5-00933-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-C5-00933-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-C5-00933-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-C5-00933-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-C5-00933-REGR | 599nm;515nm | 580nm;491nm |
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