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| Catalog: | GBAFP-CEL-10854 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CEL). 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: | CEL Gene-specific Break Apart Probe is designed to detect potential CEL 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 | Carboxyl Ester Lipase |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is a glycoprotein secreted from the pancreas into the digestive tract and from the lactating mammary gland into human milk. The physiological role of this protein is in cholesterol and lipid-soluble vitamin ester hydrolysis and absorption. This encoded protein promotes large chylomicron production in the intestine. Also its presence in plasma suggests its interactions with cholesterol and oxidized lipoproteins to modulate the progression of atherosclerosis. In pancreatic tumoral cells, this encoded protein is thought to be sequestrated within the Golgi compartment and is probably not secreted. This gene contains a variable number of tandem repeat (VNTR) polymorphism in the coding region that may influence the function of the encoded protein. [provided by RefSeq, Jul 2008] |
| Gene Symbol | CEL |
| Location | 9q34.13 |
| Chromosome | Chromosome9 |
| Coordinates | This gene maps to 135937364-135947248 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-CEL-10854-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-CEL-10854-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CEL-10854-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CEL-10854-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CEL-10854-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-CEL-10854-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-CEL-10854-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-CEL-10854-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CEL-10854-REGR | 599nm;515nm | 580nm;491nm |
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