Gene-specific Copy Number Variation Probe-CTSC
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| Catalog: |
CNVFP-CTSC-03481 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CTSC). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
CTSC Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CTSC genes. This product achieves the purpose of detection by hybridizing with the CTSC gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| 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 |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-CTSC-03481-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CTSC-03481-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CTSC-03481-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CTSC-03481-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CTSC-03481-AQ |
467nm |
418nm |
|
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