Gene-specific Copy Number Variation Probe-OVOL2
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| Catalog: |
CNVFP-OVOL2-15092 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (OVOL2). 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: |
OVOL2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to OVOL2 genes. This product achieves the purpose of detection by hybridizing with the OVOL2 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 |
Ovo Like Zinc Finger 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intrinsically disordered domains. Members of this family are involved in epithelial development and differentiation. Knockout of this gene in mouse results in early embryonic lethality with phenotypes that include neurectoderm expansion, impaired vascularization, and heart anomalies. In humans, allelic variants of this gene have been associated with posterior polymorphous corneal dystrophy. [provided by RefSeq, Apr 2016] |
| Gene Symbol |
OVOL2 |
| Location |
20p11.23 |
| Chromosome |
Chromosome20 |
| Coordinates |
This gene maps to 18004795-18038521 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-OVOL2-15092-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-OVOL2-15092-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-OVOL2-15092-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-OVOL2-15092-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-OVOL2-15092-AQ |
467nm |
418nm |
|
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