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| Catalog: | GBAFP-CFHR5-10936 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CFHR5). 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: | CFHR5 Gene-specific Break Apart Probe is designed to detect potential CFHR5 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 Factor H Related 5 |
| Gene Summary [Provided by RefSeq] | This gene is a member of a small complement factor H (CFH) gene cluster on chromosome 1. Each member of this gene family contains multiple short consensus repeats (SCRs) typical of regulators of complement activation. The protein encoded by this gene has nine SCRs with the first two repeats having heparin binding properties, a region within repeats 5-7 having heparin binding and C reactive protein binding properties, and the C-terminal repeats being similar to a complement component 3 b (C3b) binding domain. This protein co-localizes with C3, binds C3b in a dose-dependent manner, and is recruited to tissues damaged by C-reactive protein. Allelic variations in this gene have been associated, but not causally linked, with two different forms of kidney disease: membranoproliferative glomerulonephritis type II (MPGNII) and hemolytic uraemic syndrome (HUS). [provided by RefSeq, Jan 2010] |
| Gene Symbol | CFHR5 |
| Location | 1q31.3 |
| Chromosome | Chromosome1 |
| Coordinates | This gene maps to 196946686-196978808 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-CFHR5-10936-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-CFHR5-10936-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CFHR5-10936-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CFHR5-10936-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CFHR5-10936-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-CFHR5-10936-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-CFHR5-10936-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-CFHR5-10936-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CFHR5-10936-REGR | 599nm;515nm | 580nm;491nm |
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