Gene-specific Copy Number Variation Probe-SPATA18
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| Catalog: |
CNVFP-SPATA18-19717 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SPATA18). 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: |
SPATA18 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SPATA18 genes. This product achieves the purpose of detection by hybridizing with the SPATA18 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 |
Spermatogenesis Associated 18 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a p53-inducible protein that is able to induce lysosome-like organelles within mitochondria that eliminate oxidized mitochondrial proteins, thereby contributing to mitochondrial quality control. Dysregulation of mitochondrial quality control is associated with cancer and degenerative diseases. The encoded protein mediates accumulation of the lysosome-like mitochondrial organelles through interaction with B cell lymphoma 2 interacting protein 3 and B cell lymphoma 2 interacting protein 3 like at the outer mitochondrial membrane, which allows translocation of lysosomal proteins to the mitochondrial matrix from the cytosol. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016] |
| Gene Symbol |
SPATA18 |
| Location |
4q12 |
| Chromosome |
Chromosome4 |
| Coordinates |
This gene maps to 52917592-52963458 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-SPATA18-19717-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SPATA18-19717-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SPATA18-19717-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SPATA18-19717-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SPATA18-19717-AQ |
467nm |
418nm |
|
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