Gene-specific Copy Number Variation Probe-GTF2IRD1
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| Catalog: |
CNVFP-GTF2IRD1-06439 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GTF2IRD1). 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: |
GTF2IRD1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GTF2IRD1 genes. This product achieves the purpose of detection by hybridizing with the GTF2IRD1 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 |
GTF2I Repeat Domain Containing 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene plays a role in craniofacial and cognitive development and mutations have been associated with Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010] |
| Gene Symbol |
GTF2IRD1 |
| Location |
7q11.23 |
| Chromosome |
Chromosome7 |
| Coordinates |
This gene maps to 73868119-74016920 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-GTF2IRD1-06439-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GTF2IRD1-06439-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GTF2IRD1-06439-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GTF2IRD1-06439-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GTF2IRD1-06439-AQ |
467nm |
418nm |
|
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