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| Catalog: | GBAFP-BBS7-00668 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (BBS7). 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: | BBS7 Gene-specific Break Apart Probe is designed to detect potential BBS7 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 | Bardet-Biedl Syndrome 7 |
| Gene Summary [Provided by RefSeq] | This gene encodes one of eight proteins that form the BBSome complex containing BBS1, BBS2, BBS4, BBS5, BBS7, BBS8, BBS9 and BBIP10. The BBSome complex is believed to recruit Rab8(GTP) to the primary cilium and promote ciliogenesis. The BBSome complex assembly is mediated by a complex composed of three chaperonin-like BBS proteins (BBS6, BBS10, and BBS12) and CCT/TRiC family chaperonins. Mutations in this gene are implicated in Bardet-Biedl syndrome, a genetic disorder whose symptoms include obesity, retinal degeneration, polydactyly and nephropathy; however, mutations in this gene and the BBS8 gene are thought to play a minor role and mutations in chaperonin-like BBS genes are found to be a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population. Two transcript variants encoding distinct isoforms have been identified for this gene.[provided by RefSeq, Oct 2014] |
| Gene Symbol | BBS7 |
| Location | 4q27 |
| Chromosome | Chromosome4 |
| Coordinates | This gene maps to 122745483-122791652 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-BBS7-00668-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-BBS7-00668-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-BBS7-00668-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-BBS7-00668-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-BBS7-00668-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-BBS7-00668-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-BBS7-00668-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-BBS7-00668-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-BBS7-00668-REGR | 599nm;515nm | 580nm;491nm |
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