Gene-specific Copy Number Variation Probe-AIFM1
Add to Cart
| Catalog: |
CNVFP-AIFM1-00310 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (AIFM1). 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: |
AIFM1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to AIFM1 genes. This product achieves the purpose of detection by hybridizing with the AIFM1 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 |
Apoptosis Inducing Factor Mitochondria Associated 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a flavoprotein essential for nuclear disassembly in apoptotic cells, and it is found in the mitochondrial intermembrane space in healthy cells. Induction of apoptosis results in the translocation of this protein to the nucleus where it affects chromosome condensation and fragmentation. In addition, this gene product induces mitochondria to release the apoptogenic proteins cytochrome c and caspase-9. Mutations in this gene cause combined oxidative phosphorylation deficiency 6 (COXPD6), a severe mitochondrial encephalomyopathy, as well as Cowchock syndrome, also known as X-linked recessive Charcot-Marie-Tooth disease-4 (CMTX-4), a disorder resulting in neuropathy, and axonal and motor-sensory defects with deafness and cognitive disability. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 10. [provided by RefSeq, Aug 2015] |
| Gene Symbol |
AIFM1 |
| Location |
Xq26.1 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 129263337-129299861 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-AIFM1-00310-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-AIFM1-00310-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-AIFM1-00310-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-AIFM1-00310-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-AIFM1-00310-AQ |
467nm |
418nm |
|
Other Products
