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| Catalog: | GBAFP-CFI-01323 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CFI). 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: | CFI Gene-specific Break Apart Probe is designed to detect potential CFI 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 I |
| Gene Summary [Provided by RefSeq] | This gene encodes a serine proteinase that is essential for regulating the complement cascade. The encoded preproprotein is cleaved to produce both heavy and light chains, which are linked by disulfide bonds to form a heterodimeric glycoprotein. This heterodimer can cleave and inactivate the complement components C4b and C3b, and it prevents the assembly of the C3 and C5 convertase enzymes. Defects in this gene cause complement factor I deficiency, an autosomal recessive disease associated with a susceptibility to pyogenic infections. Mutations in this gene have been associated with a predisposition to atypical hemolytic uremic syndrome, a disease characterized by acute renal failure, microangiopathic hemolytic anemia and thrombocytopenia. Primary glomerulonephritis with immune deposits and age-related macular degeneration are other conditions associated with mutations of this gene. [provided by RefSeq, Dec 2015] |
| Gene Symbol | CFI |
| Location | 4q25 |
| Chromosome | Chromosome4 |
| Coordinates | This gene maps to 110661847-110723335 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-CFI-01323-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-CFI-01323-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CFI-01323-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CFI-01323-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CFI-01323-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-CFI-01323-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-CFI-01323-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-CFI-01323-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CFI-01323-REGR | 599nm;515nm | 580nm;491nm |
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