Gene-specific Copy Number Variation Probe-HTR2C
Add to Cart
| Catalog: |
CNVFP-HTR2C-07199 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HTR2C). 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: |
HTR2C Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HTR2C genes. This product achieves the purpose of detection by hybridizing with the HTR2C 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 |
5-hydroxytryptamine Receptor 2C |
| Gene Summary [Provided by RefSeq] |
This gene encodes a seven-transmembrane G-protein-coupled receptor. The encoded protein responds to signaling through the neurotransmitter serotonin. The mRNA of this gene is subject to multiple RNA editing events, where adenosine residues encoded by the genome are converted to inosines. RNA editing is predicted to alter the structure of the second intracellular loop, thereby generating alternate protein forms with decreased ability to interact with G proteins. Abnormalities in RNA editing of this gene have been detected in victims of suicide that suffer from depression. In addition, naturally-occuring variation in the promoter and 5' non-coding and coding regions of this gene may show statistically-significant association with mental illness and behavioral disorders. Alternative splicing results in multiple different transcript variants. [provided by RefSeq, Jan 2015] |
| Gene Symbol |
HTR2C |
| Location |
Xq23 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 113818550-114144624 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-HTR2C-07199-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HTR2C-07199-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HTR2C-07199-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HTR2C-07199-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HTR2C-07199-AQ |
467nm |
418nm |
|
Other Products
