Gene-specific Copy Number Variation Probe-SSX4B
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Catalog: |
CNVFP-SSX4B-19829 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SSX4B). 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: |
SSX4B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SSX4B genes. This product achieves the purpose of detection by hybridizing with the SSX4B 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 4B |
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 spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. SSX1, SSX2 and SSX4 genes have been involved in the t(X;18) translocation 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. Chromosome Xp11 contains a segmental duplication resulting in two identical copies of synovial sarcoma, X breakpoint 4, SSX4 and SSX4B, in tail-to-tail orientation. This gene, SSX4B, represents the more centromeric copy. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008] |
Gene Symbol |
SSX4B |
Location |
Xp11.23 |
Chromosome |
ChromosomeX |
Coordinates |
This gene maps to 48261527-48271344 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-SSX4B-19829-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SSX4B-19829-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SSX4B-19829-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SSX4B-19829-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SSX4B-19829-AQ |
467nm |
418nm |
|
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