Gene-specific Copy Number Variation Probe-TM4SF20
Add to Cart
| Catalog: |
CNVFP-TM4SF20-20795 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TM4SF20). 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: |
TM4SF20 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TM4SF20 genes. This product achieves the purpose of detection by hybridizing with the TM4SF20 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 |
Transmembrane 4 L Six Family Member 20 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the four-transmembrane L6 superfamily. Members of this family function in various cellular processes including cell proliferation, motility, and adhesion via their interactions with integrins. In human brain tissue, this gene is expressed at high levels in the parietal lobe, occipital lobe, hippocampus, pons, white matter, corpus callosum, and cerebellum. Knockout of the homologous gene in mouse results in a neurobehavioral phenotype with suggested enhanced motor coordination. A deletion mutation in the human gene is associated with specific language impairment-5. [provided by RefSeq, Jul 2016] |
| Gene Symbol |
TM4SF20 |
| Location |
2q36.3 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 228226873-228244022 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-TM4SF20-20795-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TM4SF20-20795-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TM4SF20-20795-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TM4SF20-20795-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TM4SF20-20795-AQ |
467nm |
418nm |
|
Other Products
