Gene-specific Copy Number Variation Probe-FMN2
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| Catalog: |
CNVFP-FMN2-05393 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FMN2). 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: |
FMN2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FMN2 genes. This product achieves the purpose of detection by hybridizing with the FMN2 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 |
Formin 2 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the formin homology protein family. The encoded protein is thought to have essential roles in organization of the actin cytoskeleton and in cell polarity. This protein mediates the formation of an actin mesh that positions the spindle during oogenesis and also regulates the formation of actin filaments in the nucleus. This protein also forms a perinuclear actin/focal-adhesion system that regulates the shape and position of the nucleus during cell migration. Mutations in this gene have been associated with infertility and also with an autosomal recessive form of intellectual disability (MRT47). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Jul 2017] |
| Gene Symbol |
FMN2 |
| Location |
1q43 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 240255184-240638489 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-FMN2-05393-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FMN2-05393-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FMN2-05393-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FMN2-05393-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FMN2-05393-AQ |
467nm |
418nm |
|
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