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| Catalog: | GBAFP-CBL-10697 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CBL). 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: | CBL Gene-specific Break Apart Probe is designed to detect potential CBL 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 | Cbl Proto-oncogene |
| Gene Summary [Provided by RefSeq] | This gene is a proto-oncogene that encodes a RING finger E3 ubiquitin ligase. The encoded protein is one of the enzymes required for targeting substrates for degradation by the proteasome. This protein mediates the transfer of ubiquitin from ubiquitin conjugating enzymes (E2) to specific substrates. This protein also contains an N-terminal phosphotyrosine binding domain that allows it to interact with numerous tyrosine-phosphorylated substrates and target them for proteasome degradation. As such it functions as a negative regulator of many signal transduction pathways. This gene has been found to be mutated or translocated in many cancers including acute myeloid leukaemia, and expansion of CGG repeats in the 5' UTR has been associated with Jacobsen syndrome. Mutations in this gene are also the cause of Noonan syndrome-like disorder. [provided by RefSeq, Jul 2016] |
| Gene Symbol | CBL |
| Location | 11q23.3 |
| Chromosome | Chromosome11 |
| Coordinates | This gene maps to 119076989-119178859 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-CBL-10697-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-CBL-10697-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CBL-10697-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CBL-10697-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CBL-10697-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-CBL-10697-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-CBL-10697-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-CBL-10697-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CBL-10697-REGR | 599nm;515nm | 580nm;491nm |
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