Gene-specific Copy Number Variation Probe-NR4A3
Add to Cart
| Catalog: |
CNVFP-NR4A3-14428 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NR4A3). 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: |
NR4A3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NR4A3 genes. This product achieves the purpose of detection by hybridizing with the NR4A3 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 4 Group A Member 3 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the steroid-thyroid hormone-retinoid receptor superfamily. The encoded protein may act as a transcriptional activator. The protein can efficiently bind the NGFI-B Response Element (NBRE). Three different versions of extraskeletal myxoid chondrosarcomas (EMCs) are the result of reciprocal translocations between this gene and other genes. The translocation breakpoints are associated with Nuclear Receptor Subfamily 4, Group A, Member 3 (on chromosome 9) and either Ewing Sarcome Breakpoint Region 1 (on chromosome 22), RNA Polymerase II, TATA Box-Binding Protein-Associated Factor, 68-KD (on chromosome 17), or Transcription factor 12 (on chromosome 15). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010] |
| Gene Symbol |
NR4A3 |
| Location |
9q31.1 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 102584136-102629173 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-NR4A3-14428-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NR4A3-14428-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NR4A3-14428-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NR4A3-14428-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NR4A3-14428-AQ |
467nm |
418nm |
|
Other Products
