Gene-specific Copy Number Variation Probe-TSIX
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| Catalog: |
CNVFP-TSIX-22291 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TSIX). 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: |
TSIX Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TSIX genes. This product achieves the purpose of detection by hybridizing with the TSIX 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 |
TSIX Transcript, XIST Antisense RNA |
| Gene Summary [Provided by RefSeq] |
In mammals, dosage compensation of genes on the X chromosome occurs by X inactivation, which is regulated in cis by the X-inactivation center (XIC) and expression of the XIST non-coding RNA. This gene expresses a non-coding antisense transcript across the 3' end of the XIST locus, and is coexpressed with XIST only from the inactive X chromosome. The mouse ortholog of this locus is required for imprinted X inactivation in extraembryonic tissues and silences Xist through modification of the chromatin structure in the Xist promoter region. In contrast, imprinted X inactivation does not occur in human extraembryonic tissues and transcripts from this locus do not repress XIST expression or affect random X chromosome inactivation in embryonic cells. This transcript is thought to be unspliced and extend over more than 30 kb, but its exact nature has not been determined. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
TSIX |
| Location |
Xq13.2 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 73012039-73049066 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-TSIX-22291-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TSIX-22291-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TSIX-22291-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TSIX-22291-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TSIX-22291-AQ |
467nm |
418nm |
|
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