Gene-specific Copy Number Variation Probe-TIMM8A
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| Catalog: |
CNVFP-TIMM8A-20874 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TIMM8A). 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: |
TIMM8A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TIMM8A genes. This product achieves the purpose of detection by hybridizing with the TIMM8A 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 |
Translocase Of Inner Mitochondrial Membrane 8A |
| Gene Summary [Provided by RefSeq] |
This translocase is involved in the import and insertion of hydrophobic membrane proteins from the cytoplasm into the mitochondrial inner membrane. The gene is mutated in Mohr-Tranebjaerg syndrome/Deafness Dystonia Syndrome (MTS/DDS) and it is postulated that MTS/DDS is a mitochondrial disease caused by a defective mitochondrial protein import system. Defects in this gene also cause Jensen syndrome; an X-linked disease with opticoacoustic nerve atrophy and muscle weakness. This protein, along with TIMM13, forms a 70 kDa heterohexamer. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Mar 2009] |
| Gene Symbol |
TIMM8A |
| Location |
Xq22.1 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 100600643-100603957 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-TIMM8A-20874-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TIMM8A-20874-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TIMM8A-20874-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TIMM8A-20874-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TIMM8A-20874-AQ |
467nm |
418nm |
|
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