Gene-specific Copy Number Variation Probe-ARHGEF9
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| Catalog: |
CNVFP-ARHGEF9-01052 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ARHGEF9). 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: |
ARHGEF9 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ARHGEF9 genes. This product achieves the purpose of detection by hybridizing with the ARHGEF9 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 |
Cdc42 Guanine Nucleotide Exchange Factor 9 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a Rho-like GTPase that switches between the active (GTP-bound) state and inactive (GDP-bound) state to regulate CDC42 and other genes. This brain-specific protein also acts as an adaptor protein for the recruitment of gephyrin and together these proteins facilitate receceptor recruitement in GABAnergic and glycinergic synapses. Defects in this gene are the cause of startle disease with epilepsy (STHEE), also known as hyperekplexia with epilepsy, as well as several other types of cognitive disability. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017] |
| Gene Symbol |
ARHGEF9 |
| Location |
Xq11.1 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 62854847-63005426 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-ARHGEF9-01052-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ARHGEF9-01052-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ARHGEF9-01052-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ARHGEF9-01052-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ARHGEF9-01052-AQ |
467nm |
418nm |
|
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