Gene-specific Copy Number Variation Probe-CAPNS1
Add to Cart
| Catalog: |
CNVFP-CAPNS1-01992 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CAPNS1). 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: |
CAPNS1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CAPNS1 genes. This product achieves the purpose of detection by hybridizing with the CAPNS1 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 |
Calpain Small Subunit 1 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the calpain small subunit family. Calpains are calcium-dependent cysteine proteinases that are widely distributed in mammalian cells. Calpains operate as heterodimers, comprising a specific large catalytic subunit (calpain 1 subunit in Calpain I, and calpain 2 subunit in Calpain II), and a common small regulatory subunit encoded by this gene. This encoded protein is essential for the stability and function of both calpain heterodimers, whose proteolytic activities influence various cellular functions including apoptosis, proliferation, migration, adhesion, and autophagy. Calpains have been implicated in neurodegenerative processes, such as myotonic dystrophy. A pseudogene of this gene has been defined on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014] |
| Gene Symbol |
CAPNS1 |
| Location |
19q13.12 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 36630917-36641255 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-CAPNS1-01992-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CAPNS1-01992-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CAPNS1-01992-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CAPNS1-01992-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CAPNS1-01992-AQ |
467nm |
418nm |
|
Other Products
