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| Catalog: | GBAFP-MBD5-13908 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (MBD5). 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: | MBD5 Gene-specific Break Apart Probe is designed to detect potential MBD5 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 | Methyl-CpG Binding Domain Protein 5 |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the methyl-CpG-binding domain (MBD) family. The MBD consists of about 70 residues and is the minimal region required for a methyl-CpG-binding protein binding specifically to methylated DNA. In addition to the MBD domain, this protein contains a PWWP domain (Pro-Trp-Trp-Pro motif), which consists of 100-150 amino acids and is found in numerous proteins that are involved in cell division, growth and differentiation. Mutations in this gene cause an autosomal dominant type of cognitive disability. The encoded protein interacts with the polycomb repressive complex PR-DUB which catalyzes the deubiquitination of a lysine residue of histone 2A. Haploinsufficiency of this gene is associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures. Alternatively spliced transcript variants have been found, but their full-length nature is not determined. [provided by RefSeq, Jul 2017] |
| Gene Symbol | MBD5 |
| Location | 2q23.1 |
| Chromosome | Chromosome2 |
| Coordinates | This gene maps to 148778579-149271044 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-MBD5-13908-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-MBD5-13908-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-MBD5-13908-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-MBD5-13908-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-MBD5-13908-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-MBD5-13908-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-MBD5-13908-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-MBD5-13908-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-MBD5-13908-REGR | 599nm;515nm | 580nm;491nm |
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