Gene-specific Copy Number Variation Probe-FGF8
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| Catalog: |
CNVFP-FGF8-05377 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FGF8). 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: |
FGF8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FGF8 genes. This product achieves the purpose of detection by hybridizing with the FGF8 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 8 |
| 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 is known to be a factor that supports androgen and anchorage independent growth of mammary tumor cells. Overexpression of this gene has been shown to increase tumor growth and angiogensis. The adult expression of this gene is restricted to testes and ovaries. Temporal and spatial pattern of this gene expression suggests its function as an embryonic epithelial factor. Studies of the mouse and chick homologs revealed roles in midbrain and limb development, organogenesis, embryo gastrulation and left-right axis determination. The alternative splicing of this gene results in four transcript variants. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
FGF8 |
| Location |
10q24.32 |
| Chromosome |
Chromosome10 |
| Coordinates |
This gene maps to 103529886-103540126 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-FGF8-05377-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FGF8-05377-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FGF8-05377-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FGF8-05377-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FGF8-05377-AQ |
467nm |
418nm |
|
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