Gene-specific Copy Number Variation Probe-FGF17
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| Catalog: |
CNVFP-FGF17-05477 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FGF17). 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: |
FGF17 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FGF17 genes. This product achieves the purpose of detection by hybridizing with the FGF17 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 17 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the fibroblast growth factor (FGF) family. Member of the FGF family 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 expressed during embryogenesis and in the adult cerebellum and cortex and may be essential for vascular growth and normal brain development. Mutations in this gene are the cause of hypogonadotropic hypogonadism 20 with or without anosmia. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015] |
| Gene Symbol |
FGF17 |
| Location |
8p21.3 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 21900427-21906319 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-FGF17-05477-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FGF17-05477-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FGF17-05477-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FGF17-05477-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FGF17-05477-AQ |
467nm |
418nm |
|
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