Gene-specific Copy Number Variation Probe-FGF2
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| Catalog: |
CNVFP-FGF2-05476 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FGF2). 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: |
FGF2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FGF2 genes. This product achieves the purpose of detection by hybridizing with the FGF2 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 2 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members bind heparin and possess broad mitogenic and angiogenic activities. This protein has been implicated in diverse biological processes, such as limb and nervous system development, wound healing, and tumor growth. The mRNA for this gene contains multiple polyadenylation sites, and is alternatively translated from non-AUG (CUG) and AUG initiation codons, resulting in five different isoforms with distinct properties. The CUG-initiated isoforms are localized in the nucleus and are responsible for the intracrine effect, whereas, the AUG-initiated form is mostly cytosolic and is responsible for the paracrine and autocrine effects of this FGF. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
FGF2 |
| Location |
4q28.1 |
| Chromosome |
Chromosome4 |
| Coordinates |
This gene maps to 123747862-123819390 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-FGF2-05476-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FGF2-05476-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FGF2-05476-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FGF2-05476-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FGF2-05476-AQ |
467nm |
418nm |
|
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