Gene-specific Copy Number Variation Probe-NKX2-8
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| Catalog: |
CNVFP-NKX2-8-14302 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NKX2-8). 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: |
NKX2-8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NKX2-8 genes. This product achieves the purpose of detection by hybridizing with the NKX2-8 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 |
NK2 Homeobox 8 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a homeobox-containing developmental regulator associated with liver development. The encoded protein binds to the alpha-fetoprotein (AFP) gene promoter and increases the expression of AFP. This gene is overexpressed in some lung cancers and is linked to poor patient survival, possibly due to its resistance to cisplatin. This gene is aberrantly methylated in pancreatic cancer, deleted in squamous cell lung carcinomas, and acts as a tumor suppressor in esophageal cancer. Mutations in this gene may also be a cause of neural tube defects. [provided by RefSeq, Dec 2015] |
| Gene Symbol |
NKX2-8 |
| Location |
14q13.3 |
| Chromosome |
Chromosome14 |
| Coordinates |
This gene maps to 37049215-37051786 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-NKX2-8-14302-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NKX2-8-14302-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NKX2-8-14302-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NKX2-8-14302-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NKX2-8-14302-AQ |
467nm |
418nm |
|
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