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| Catalog: | GBAFP-CREBBP-01617 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CREBBP). 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: | CREBBP Gene-specific Break Apart Probe is designed to detect potential CREBBP 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 | CREB Binding Protein |
| Gene Summary [Provided by RefSeq] | This gene is ubiquitously expressed and is involved in the transcriptional coactivation of many different transcription factors. First isolated as a nuclear protein that binds to cAMP-response element binding protein (CREB), this gene is now known to play critical roles in embryonic development, growth control, and homeostasis by coupling chromatin remodeling to transcription factor recognition. The protein encoded by this gene has intrinsic histone acetyltransferase activity and also acts as a scaffold to stabilize additional protein interactions with the transcription complex. This protein acetylates both histone and non-histone proteins. This protein shares regions of very high sequence similarity with protein p300 in its bromodomain, cysteine-histidine-rich regions, and histone acetyltransferase domain. Mutations in this gene cause Rubinstein-Taybi syndrome (RTS). Chromosomal translocations involving this gene have been associated with acute myeloid leukemia. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2009] |
| Gene Symbol | CREBBP |
| Location | 16p13.3 |
| Chromosome | Chromosome16 |
| Coordinates | This gene maps to 3775055-3930121 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-CREBBP-01617-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-CREBBP-01617-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CREBBP-01617-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CREBBP-01617-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CREBBP-01617-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-CREBBP-01617-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-CREBBP-01617-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-CREBBP-01617-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CREBBP-01617-REGR | 599nm;515nm | 580nm;491nm |
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