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| Catalog: | GBAFP-PLCE1-15912 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (PLCE1). 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: | PLCE1 Gene-specific Break Apart Probe is designed to detect potential PLCE1 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 | Phospholipase C Epsilon 1 |
| Gene Summary [Provided by RefSeq] | This gene encodes a phospholipase enzyme that catalyzes the hydrolysis of phosphatidylinositol-4,5-bisphosphate to generate two second messengers: inositol 1,4,5-triphosphate (IP3) and diacylglycerol (DAG). These second messengers subsequently regulate various processes affecting cell growth, differentiation, and gene expression. This enzyme is regulated by small monomeric GTPases of the Ras and Rho families and by heterotrimeric G proteins. In addition to its phospholipase C catalytic activity, this enzyme has an N-terminal domain with guanine nucleotide exchange (GEF) activity. Mutations in this gene cause early-onset nephrotic syndrome; characterized by proteinuria, edema, and diffuse mesangial sclerosis or focal and segmental glomerulosclerosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Sep 2009] |
| Gene Symbol | PLCE1 |
| Location | 10q23.33 |
| Chromosome | Chromosome10 |
| Coordinates | This gene maps to 95753745-96088148 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-PLCE1-15912-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-PLCE1-15912-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-PLCE1-15912-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-PLCE1-15912-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-PLCE1-15912-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-PLCE1-15912-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-PLCE1-15912-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-PLCE1-15912-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-PLCE1-15912-REGR | 599nm;515nm | 580nm;491nm |
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