Gene-specific Copy Number Variation Probe-FOXN1
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| Catalog: |
CNVFP-FOXN1-05607 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FOXN1). 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: |
FOXN1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FOXN1 genes. This product achieves the purpose of detection by hybridizing with the FOXN1 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 |
Forkhead Box N1 |
| Gene Summary [Provided by RefSeq] |
Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
FOXN1 |
| Location |
17q11.2 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 26850958-26865175 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-FOXN1-05607-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FOXN1-05607-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FOXN1-05607-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FOXN1-05607-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FOXN1-05607-AQ |
467nm |
418nm |
|
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