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| Catalog: | GBAFP-MKKS-05169 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (MKKS). 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: | MKKS Gene-specific Break Apart Probe is designed to detect potential MKKS 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 | McKusick-Kaufman Syndrome |
| Gene Summary [Provided by RefSeq] | This gene encodes a protein which shares sequence similarity with other members of the type II chaperonin family. The encoded protein is a centrosome-shuttling protein and plays an important role in cytokinesis. This protein also interacts with other type II chaperonin members to form a complex known as the BBSome, which involves ciliary membrane biogenesis. This protein is encoded by a downstream open reading frame (dORF). Several upstream open reading frames (uORFs) have been identified, which repress the translation of the dORF, and two of which can encode small mitochondrial membrane proteins. Mutations in this gene have been observed in patients with Bardet-Biedl syndrome type 6, also known as McKusick-Kaufman syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013] |
| Gene Symbol | MKKS |
| Location | 20p12.2 |
| Chromosome | Chromosome20 |
| Coordinates | This gene maps to 10385832-10414866 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-MKKS-05169-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-MKKS-05169-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-MKKS-05169-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-MKKS-05169-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-MKKS-05169-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-MKKS-05169-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-MKKS-05169-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-MKKS-05169-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-MKKS-05169-REGR | 599nm;515nm | 580nm;491nm |
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