Gene-specific Copy Number Variation Probe-FGD1
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| Catalog: |
CNVFP-FGD1-05223 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FGD1). 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: |
FGD1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FGD1 genes. This product achieves the purpose of detection by hybridizing with the FGD1 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 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein that contains Dbl (DH) and pleckstrin (PH) homology domains and is similar to the Rho family of small GTP-binding proteins. The encoded protein specifically binds to the Rho family GTPase Cdc42Hs and can stimulate the GDP-GTP exchange of the isoprenylated form of Cdc42Hs. It also stimulates the mitogen activated protein kinase cascade leading to c-Jun kinase SAPK/JNK1 activation. Defects in this gene are the cause of the faciogenital dysplasia in Aarskog-Scott syndrome and a syndromatic form of X-linked cognitive disability. [provided by RefSeq, Jul 2017] |
| Gene Symbol |
FGD1 |
| Location |
Xp11.22 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 54471886-54522599 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-FGD1-05223-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FGD1-05223-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FGD1-05223-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FGD1-05223-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FGD1-05223-AQ |
467nm |
418nm |
|
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