Gene-specific Copy Number Variation Probe-FGD4
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| Catalog: |
CNVFP-FGD4-05221 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FGD4). 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: |
FGD4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FGD4 genes. This product achieves the purpose of detection by hybridizing with the FGD4 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 |
FYVE, RhoGEF And PH Domain Containing 4 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein that is involved in the regulation of the actin cytoskeleton and cell shape. This protein contains an actin filament-binding domain, which together with its Dbl homology domain and one of its pleckstrin homology domains, can form microspikes. This protein can activate MAPK8 independently of the actin filament-binding domain, and it is also involved in the activation of CDC42 via the exchange of bound GDP for free GTP. The activation of CDC42 also enables this protein to play a role in mediating the cellular invasion of Cryptosporidium parvum, an intracellular parasite that infects the gastrointestinal tract. Mutations in this gene can cause Charcot-Marie-Tooth disease type 4H (CMT4H), a disorder of the peripheral nervous system. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015] |
| Gene Symbol |
FGD4 |
| Location |
12p11.21 |
| Chromosome |
Chromosome12 |
| Coordinates |
This gene maps to 32655040-32798984 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-FGD4-05221-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FGD4-05221-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FGD4-05221-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FGD4-05221-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FGD4-05221-AQ |
467nm |
418nm |
|
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