Gene-specific Copy Number Variation Probe-GSC2
Add to Cart
| Catalog: |
CNVFP-GSC2-06491 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GSC2). 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: |
GSC2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GSC2 genes. This product achieves the purpose of detection by hybridizing with the GSC2 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 |
Goosecoid Homeobox 2 |
| Gene Summary [Provided by RefSeq] |
Goosecoidlike (GSCL), a homeodomain-containing gene, resides in the critical region for VCFS/DGS on 22q11. Velocardiofacial syndrome (VCFS) is a developmental disorder characterized by conotruncal heart defects, craniofacial anomalies, and learning disabilities. VCFS is phenotypically related to DiGeorge syndrome (DGS) and both syndromes are associated with hemizygous 22q11 deletions. Because many of the tissues and structures affected in VCFS/DGS derive from the pharyngeal arches of the developing embryo, it is believed that haploinsufficiency of a gene involved in embryonic development may be responsible for its etiology. The gene is expressed in a limited number of adult tissues, as well as in early human development. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
GSC2 |
| Location |
22q11.21 |
| Chromosome |
Chromosome22 |
| Coordinates |
This gene maps to 19136503-19137796 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-GSC2-06491-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GSC2-06491-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GSC2-06491-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GSC2-06491-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GSC2-06491-AQ |
467nm |
418nm |
|
Other Products
