Gene-specific Copy Number Variation Probe-TOM1L2
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| Catalog: |
CNVFP-TOM1L2-21195 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TOM1L2). 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: |
TOM1L2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TOM1L2 genes. This product achieves the purpose of detection by hybridizing with the TOM1L2 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 |
Target Of Myb1 Like 2 Membrane Trafficking Protein |
| Gene Summary [Provided by RefSeq] |
This gene belongs to a small gene family whose members have an N-terminal VHS domain followed by a GAT domain; domains which typically participate in vesicular trafficking. The canonical protein encoded by this gene also has a C-terminal clathrin binding motif. This protein has been shown to interact with Tollip, clathrin and ubiquitin and is thought to play a role in endosomal sorting. This gene resides in the 3.7 Mb deletion of chromosome region 17p11.2 that is associated with Smith-Magenis syndrome. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Apr 2017] |
| Gene Symbol |
TOM1L2 |
| Location |
17p11.2 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 17746821-17875784 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-TOM1L2-21195-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TOM1L2-21195-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TOM1L2-21195-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TOM1L2-21195-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TOM1L2-21195-AQ |
467nm |
418nm |
|
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