Gene-specific Copy Number Variation Probe-ESS2
Add to Cart
| Catalog: |
CNVFP-ESS2-04716 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ESS2). 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: |
ESS2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ESS2 genes. This product achieves the purpose of detection by hybridizing with the ESS2 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 |
Ess-2 Splicing Factor Homolog |
| Gene Summary [Provided by RefSeq] |
This gene is located within the minimal DGS critical region (MDGCR) thought to contain the gene(s) responsible for a group of developmental disorders. These disorders include DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome, and some familial or sporadic conotruncal cardiac defects which have been associated with microdeletion of 22q11.2. The encoded protein may be a component of C complex spliceosomes, and the orthologous protein in the mouse localizes to the nucleus. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2015] |
| Gene Symbol |
ESS2 |
| Location |
22q11.2 |
| Chromosome |
Chromosome22 |
| Coordinates |
This gene maps to 19144725-19130278 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-ESS2-04716-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ESS2-04716-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ESS2-04716-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ESS2-04716-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ESS2-04716-AQ |
467nm |
418nm |
|
Other Products
