Gene-specific Copy Number Variation Probe-RFX2
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| Catalog: |
CNVFP-RFX2-17169 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RFX2). 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: |
RFX2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RFX2 genes. This product achieves the purpose of detection by hybridizing with the RFX2 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 |
Regulatory Factor X2 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the regulatory factor X gene family, which encodes transcription factors that contain a highly-conserved winged helix DNA binding domain. The protein encoded by this gene is structurally related to regulatory factors X1, X3, X4, and X5. It is a transcriptional activator that can bind DNA as a monomer or as a heterodimer with other RFX family members. This protein can bind to cis elements in the promoter of the IL-5 receptor alpha gene. Two transcript variants encoding different isoforms have been described for this gene, and both variants utilize alternative polyadenylation sites. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
RFX2 |
| Location |
19p13.3 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 5993174-6110664 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-RFX2-17169-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RFX2-17169-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RFX2-17169-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RFX2-17169-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RFX2-17169-AQ |
467nm |
418nm |
|
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