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| Catalog: | GBAFP-CYP21A2-11337 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CYP21A2). 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: | CYP21A2 Gene-specific Break Apart Probe is designed to detect potential CYP21A2 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 | Cytochrome P450 Family 21 Subfamily A Member 2 |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and hydroxylates steroids at the 21 position. Its activity is required for the synthesis of steroid hormones including cortisol and aldosterone. Mutations in this gene cause congenital adrenal hyperplasia. A related pseudogene is located near this gene; gene conversion events involving the functional gene and the pseudogene are thought to account for many cases of steroid 21-hydroxylase deficiency. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol | CYP21A2 |
| Location | 6p21.33 |
| Chromosome | Chromosome6_ssto_hap7 |
| Coordinates | This gene maps to 3306068-3342155 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-CYP21A2-11337-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-CYP21A2-11337-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CYP21A2-11337-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CYP21A2-11337-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CYP21A2-11337-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-CYP21A2-11337-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-CYP21A2-11337-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-CYP21A2-11337-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CYP21A2-11337-REGR | 599nm;515nm | 580nm;491nm |
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