Gene-specific Copy Number Variation Probe-TWNK
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| Catalog: |
CNVFP-TWNK-22638 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TWNK). 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: |
TWNK Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TWNK genes. This product achieves the purpose of detection by hybridizing with the TWNK 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 |
Twinkle MtDNA Helicase |
| Gene Summary [Provided by RefSeq] |
This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5' to 3' direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Aug 2009] |
| Gene Symbol |
TWNK |
| Location |
10q24.31 |
| Chromosome |
Chromosome10 |
| Coordinates |
This gene maps to 100987526-100994402 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-TWNK-22638-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TWNK-22638-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TWNK-22638-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TWNK-22638-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TWNK-22638-AQ |
467nm |
418nm |
|
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