Gene-specific Copy Number Variation Probe-TBL1X
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| Catalog: |
CNVFP-TBL1X-20410 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TBL1X). 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: |
TBL1X Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TBL1X genes. This product achieves the purpose of detection by hybridizing with the TBL1X 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 |
Transducin Beta Like 1 X-linked |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This encoded protein is found as a subunit in corepressor SMRT (silencing mediator for retinoid and thyroid receptors) complex along with histone deacetylase 3 protein. This gene is located adjacent to the ocular albinism gene and it is thought to be involved in the pathogenesis of the ocular albinism with late-onset sensorineural deafness phenotype. Four transcript variants encoding two different isoforms have been found for this gene. This gene is highly similar to the Y chromosome TBL1Y gene. [provided by RefSeq, Nov 2008] |
| Gene Symbol |
TBL1X |
| Location |
Xp22.31-p22.2 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 9431334-9687780 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-TBL1X-20410-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TBL1X-20410-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TBL1X-20410-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TBL1X-20410-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TBL1X-20410-AQ |
467nm |
418nm |
|
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