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| Catalog: | GBAFP-HFE2-12734 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (HFE2). 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: | HFE2 Gene-specific Break Apart Probe is designed to detect potential HFE2 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 | Hemochromatosis Type 2 (juvenile) |
| Gene Summary [Provided by RefSeq] | The product of this gene is involved in iron metabolism. It may be a component of the signaling pathway which activates hepcidin or it may act as a modulator of hepcidin expression. It could also represent the cellular receptor for hepcidin. Two uORFs in the 5' UTR negatively regulate the expression and activity of the encoded protein. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. Defects in this gene are the cause of hemochromatosis type 2A, also called juvenile hemochromatosis (JH). JH is an early-onset autosomal recessive disorder due to severe iron overload resulting in hypogonadotrophic hypogonadism, hepatic fibrosis or cirrhosis and cardiomyopathy, occurring typically before age of 30. [provided by RefSeq, Oct 2015] |
| Gene Symbol | HFE2 |
| Location | 1q21.1 |
| Chromosome | Chromosome1 |
| Coordinates | This gene maps to 145413190-145417545 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-HFE2-12734-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-HFE2-12734-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-HFE2-12734-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-HFE2-12734-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-HFE2-12734-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-HFE2-12734-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-HFE2-12734-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-HFE2-12734-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-HFE2-12734-REGR | 599nm;515nm | 580nm;491nm |
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