Gene-specific Copy Number Variation Probe-NR3C2
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Catalog: |
CNVFP-NR3C2-14433 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NR3C2). 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: |
NR3C2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NR3C2 genes. This product achieves the purpose of detection by hybridizing with the NR3C2 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 3 Group C Member 2 |
Gene Summary [Provided by RefSeq] |
This gene encodes the mineralocorticoid receptor, which mediates aldosterone actions on salt and water balance within restricted target cells. The protein functions as a ligand-dependent transcription factor that binds to mineralocorticoid response elements in order to transactivate target genes. Mutations in this gene cause autosomal dominant pseudohypoaldosteronism type I, a disorder characterized by urinary salt wasting. Defects in this gene are also associated with early onset hypertension with severe exacerbation in pregnancy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009] |
Gene Symbol |
NR3C2 |
Location |
4q31.23 |
Chromosome |
Chromosome4 |
Coordinates |
This gene maps to 148999914-149363672 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-NR3C2-14433-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-NR3C2-14433-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-NR3C2-14433-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-NR3C2-14433-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-NR3C2-14433-AQ |
467nm |
418nm |
|
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