Gene-specific Copy Number Variation Probe-TSPAN32
Add to Cart
| Catalog: |
CNVFP-TSPAN32-22250 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TSPAN32). 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: |
TSPAN32 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TSPAN32 genes. This product achieves the purpose of detection by hybridizing with the TSPAN32 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 |
Tetraspanin 32 |
| Gene Summary [Provided by RefSeq] |
This gene, which is a member of the tetraspanin superfamily, is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of chromosome 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian and breast cancers. This gene is located among several imprinted genes; however, this gene, as well as the tumor-suppressing subchromosomal transferable fragment 4, escapes imprinting. This gene may play a role in malignancies and diseases that involve this region, and it is also involved in hematopoietic cell function. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
TSPAN32 |
| Location |
11p15.5 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 2323242-2339430 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-TSPAN32-22250-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TSPAN32-22250-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TSPAN32-22250-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TSPAN32-22250-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TSPAN32-22250-AQ |
467nm |
418nm |
|
Other Products
