Gene-specific Copy Number Variation Probe-SSX2
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| Catalog: |
CNVFP-SSX2-19860 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SSX2). 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: |
SSX2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SSX2 genes. This product achieves the purpose of detection by hybridizing with the SSX2 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 |
SSX Family Member 2 |
| Gene Summary [Provided by RefSeq] |
The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneous humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. This gene, and also the SSX1 and SSX4 family members, have been involved in t(X;18)(p11.2;q11.2) translocations that are characteristically found in all synovial sarcomas. This translocation results in the fusion of the synovial sarcoma translocation gene on chromosome 18 to one of the SSX genes on chromosome X. The encoded hybrid proteins are likely responsible for transforming activity. Alternative splicing of this gene results in multiple transcript variants. This gene also has an identical duplicate, GeneID: 727837, located about 45 kb downstream in the opposite orientation on chromosome X. [provided by RefSeq, Jul 2013] |
| Gene Symbol |
SSX2 |
| Location |
Xp11.22 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 52780307-52790617 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-SSX2-19860-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SSX2-19860-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SSX2-19860-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SSX2-19860-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SSX2-19860-AQ |
467nm |
418nm |
|
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