Gene-specific Copy Number Variation Probe-GTF2H2
Add to Cart
| Catalog: |
CNVFP-GTF2H2-06446 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GTF2H2). 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: |
GTF2H2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GTF2H2 genes. This product achieves the purpose of detection by hybridizing with the GTF2H2 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 |
General Transcription Factor IIH Subunit 2 |
| Gene Summary [Provided by RefSeq] |
This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is within the telomeric copy of the duplication. Deletion of this gene sometimes accompanies deletion of the neighboring SMN1 gene in spinal muscular atrophy (SMA) patients but it is unclear if deletion of this gene contributes to the SMA phenotype. This gene encodes the 44 kDa subunit of RNA polymerase II transcription initiation factor IIH which is involved in basal transcription and nucleotide excision repair. Transcript variants for this gene have been described, but their full length nature has not been determined. A second copy of this gene within the centromeric copy of the duplication has been described in the literature. It is reported to be different by either two or four base pairs; however, no sequence data is currently available for the centromeric copy of the gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
GTF2H2 |
| Location |
5q13.2 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 70330950-70363497 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-GTF2H2-06446-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GTF2H2-06446-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GTF2H2-06446-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GTF2H2-06446-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GTF2H2-06446-AQ |
467nm |
418nm |
|
Other Products
