Gene-specific Copy Number Variation Probe-NR2C2
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| Catalog: |
CNVFP-NR2C2-14457 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NR2C2). 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: |
NR2C2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NR2C2 genes. This product achieves the purpose of detection by hybridizing with the NR2C2 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 |
Nuclear Receptor Subfamily 2 Group C Member 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein that belongs to the nuclear hormone receptor family. Members of this family act as ligand-activated transcription factors and function in many biological processes such as development, cellular differentiation and homeostasis. The activated receptor/ligand complex is translocated to the nucleus where it binds to hormone response elements of target genes. The protein encoded by this gene plays a role in protecting cells from oxidative stress and damage induced by ionizing radiation. The lack of a similar gene in mouse results in growth retardation, severe spinal curvature, subfertility, premature aging, and prostatic intraepithelial neoplasia (PIN) development. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2014] |
| Gene Symbol |
NR2C2 |
| Location |
3p25.1 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 14989235-15090780 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-NR2C2-14457-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NR2C2-14457-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NR2C2-14457-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NR2C2-14457-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NR2C2-14457-AQ |
467nm |
418nm |
|
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