Gene-specific Copy Number Variation Probe-FGF9
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| Catalog: |
CNVFP-FGF9-05376 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FGF9). 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: |
FGF9 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FGF9 genes. This product achieves the purpose of detection by hybridizing with the FGF9 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 |
Fibroblast Growth Factor 9 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein was isolated as a secreted factor that exhibits a growth-stimulating effect on cultured glial cells. In nervous system, this protein is produced mainly by neurons and may be important for glial cell development. Expression of the mouse homolog of this gene was found to be dependent on Sonic hedgehog (Shh) signaling. Mice lacking the homolog gene displayed a male-to-female sex reversal phenotype, which suggested a role in testicular embryogenesis. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
FGF9 |
| Location |
13q12.11 |
| Chromosome |
Chromosome13 |
| Coordinates |
This gene maps to 22245214-22278640 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-FGF9-05376-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FGF9-05376-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FGF9-05376-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FGF9-05376-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FGF9-05376-AQ |
467nm |
418nm |
|
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