Gene-specific Copy Number Variation Probe-FGF20
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| Catalog: |
CNVFP-FGF20-05474 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FGF20). 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: |
FGF20 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FGF20 genes. This product achieves the purpose of detection by hybridizing with the FGF20 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 20 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the fibroblast growth factor family. The fibroblast growth factors 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 gene product is a secreted neurotrophic factor but lacks a typical signal peptide. It is expressed in normal brain, particularly the cerebellum, and may regulate central nervous system development and function. Homodimerization of this protein was shown to regulate its receptor binding activity and concentration gradient in the extracellular matrix. Genetic variations of this gene have been associated with Parkinson disease susceptibility. [provided by RefSeq, Oct 2009] |
| Gene Symbol |
FGF20 |
| Location |
8p22 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 16850333-16859674 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-FGF20-05474-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FGF20-05474-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FGF20-05474-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FGF20-05474-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FGF20-05474-AQ |
467nm |
418nm |
|
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