Gene-specific Copy Number Variation Probe-ASAH1
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| Catalog: |
CNVFP-ASAH1-00981 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ASAH1). 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: |
ASAH1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ASAH1 genes. This product achieves the purpose of detection by hybridizing with the ASAH1 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 |
N-acylsphingosine Amidohydrolase 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the acid ceramidase family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. Processing of this preproprotein generates alpha and beta subunits that heterodimerize to form the mature lysosomal enzyme, which catalyzes the degradation of ceramide into sphingosine and free fatty acid. This enzyme is overexpressed in multiple human cancers and may play a role in cancer progression. Mutations in this gene are associated with the lysosomal storage disorder, Farber lipogranulomatosis, and a neuromuscular disorder, spinal muscular atrophy with progressive myoclonic epilepsy. [provided by RefSeq, Oct 2015] |
| Gene Symbol |
ASAH1 |
| Location |
8p22 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 17913924-17942507 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-ASAH1-00981-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ASAH1-00981-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ASAH1-00981-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ASAH1-00981-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ASAH1-00981-AQ |
467nm |
418nm |
|
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