CONTACT SUPPORT
Online Inquiry
| Catalog: | GBAFP-CTSB-01668 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CTSB). 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: | CTSB Gene-specific Break Apart Probe is designed to detect potential CTSB 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 B |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the C1 family of peptidases. Alternative splicing of this gene results in multiple transcript variants. At least one of these variants encodes a preproprotein that is proteolytically processed to generate multiple protein products. These products include the cathepsin B light and heavy chains, which can dimerize to form the double chain form of the enzyme. This enzyme is a lysosomal cysteine protease with both endopeptidase and exopeptidase activity that may play a role in protein turnover. It is also known as amyloid precursor protein secretase and is involved in the proteolytic processing of amyloid precursor protein (APP). Incomplete proteolytic processing of APP has been suggested to be a causative factor in Alzheimer's disease, the most common cause of dementia. Overexpression of the encoded protein has been associated with esophageal adenocarcinoma and other tumors. Multiple pseudogenes of this gene have been identified. [provided by RefSeq, Nov 2015] |
| Gene Symbol | CTSB |
| Location | 8p23.1 |
| Chromosome | Chromosome8 |
| Coordinates | This gene maps to 11700033-11725646 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-CTSB-01668-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-CTSB-01668-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CTSB-01668-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CTSB-01668-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CTSB-01668-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-CTSB-01668-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-CTSB-01668-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-CTSB-01668-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CTSB-01668-REGR | 599nm;515nm | 580nm;491nm |
Other Products