Gene-specific Copy Number Variation Probe-TBX1
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| Catalog: |
CNVFP-TBX1-20399 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TBX1). 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: |
TBX1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TBX1 genes. This product achieves the purpose of detection by hybridizing with the TBX1 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 |
T-box 1 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product shares 98% amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
TBX1 |
| Location |
22q11.21 |
| Chromosome |
Chromosome22 |
| Coordinates |
This gene maps to 19744225-19771112 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-TBX1-20399-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TBX1-20399-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TBX1-20399-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TBX1-20399-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TBX1-20399-AQ |
467nm |
418nm |
|
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