CONTACT SUPPORT
Online Inquiry
| Catalog: | GBAFP-CSTB-01688 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CSTB). 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: | CSTB Gene-specific Break Apart Probe is designed to detect potential CSTB 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 | Cystatin B |
| Gene Summary [Provided by RefSeq] | The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and kininogens. This gene encodes a stefin that functions as an intracellular thiol protease inhibitor. The protein is able to form a dimer stabilized by noncovalent forces, inhibiting papain and cathepsins l, h and b. The protein is thought to play a role in protecting against the proteases leaking from lysosomes. Evidence indicates that mutations in this gene are responsible for the primary defects in patients with progressive myoclonic epilepsy (EPM1). One type of mutation responsible for EPM1 is the expansion in the promoter region of this gene of a CCCCGCCCCGCG repeat from 2-3 copies to 30-78 copies. [provided by RefSeq, Jul 2016] |
| Gene Symbol | CSTB |
| Location | 21q22.3 |
| Chromosome | Chromosome21 |
| Coordinates | This gene maps to 45193830-45196259 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-CSTB-01688-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-CSTB-01688-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CSTB-01688-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CSTB-01688-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CSTB-01688-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-CSTB-01688-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-CSTB-01688-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-CSTB-01688-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CSTB-01688-REGR | 599nm;515nm | 580nm;491nm |
Other Products