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| Catalog: | GBAFP-CTSC-01667 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CTSC). 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: | CTSC Gene-specific Break Apart Probe is designed to detect potential CTSC 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 | Cathepsin C |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the peptidase C1 family and lysosomal cysteine proteinase that appears to be a central coordinator for activation of many serine proteinases in cells of the immune system. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate heavy and light chains that form a disulfide-linked dimer. A portion of the propeptide acts as an intramolecular chaperone for the folding and stabilization of the mature enzyme. This enzyme requires chloride ions for activity and can degrade glucagon. Defects in the encoded protein have been shown to be a cause of Papillon-Lefevre syndrome, an autosomal recessive disorder characterized by palmoplantar keratosis and periodontitis. [provided by RefSeq, Nov 2015] |
| Gene Symbol | CTSC |
| Location | 11q14.2 |
| Chromosome | Chromosome11 |
| Coordinates | This gene maps to 88026759-88070941 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-CTSC-01667-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-CTSC-01667-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CTSC-01667-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CTSC-01667-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CTSC-01667-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-CTSC-01667-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-CTSC-01667-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-CTSC-01667-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CTSC-01667-REGR | 599nm;515nm | 580nm;491nm |
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