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| Catalog: | GBAFP-HMGCR-12919 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (HMGCR). 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: | HMGCR Gene-specific Break Apart Probe is designed to detect potential HMGCR 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 | 3-hydroxy-3-methylglutaryl-CoA Reductase |
| Gene Summary [Provided by RefSeq] | HMG-CoA reductase is the rate-limiting enzyme for cholesterol synthesis and is regulated via a negative feedback mechanism mediated by sterols and non-sterol metabolites derived from mevalonate, the product of the reaction catalyzed by reductase. Normally in mammalian cells this enzyme is suppressed by cholesterol derived from the internalization and degradation of low density lipoprotein (LDL) via the LDL receptor. Competitive inhibitors of the reductase induce the expression of LDL receptors in the liver, which in turn increases the catabolism of plasma LDL and lowers the plasma concentration of cholesterol, an important determinant of atherosclerosis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008] |
| Gene Symbol | HMGCR |
| Location | 5q13.3 |
| Chromosome | Chromosome5 |
| Coordinates | This gene maps to 74632992-74657926 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-HMGCR-12919-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-HMGCR-12919-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-HMGCR-12919-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-HMGCR-12919-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-HMGCR-12919-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-HMGCR-12919-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-HMGCR-12919-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-HMGCR-12919-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-HMGCR-12919-REGR | 599nm;515nm | 580nm;491nm |
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