Gene-specific Copy Number Variation Probe-CHRND
Add to Cart
| Catalog: |
CNVFP-CHRND-02824 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CHRND). 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: |
CHRND Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CHRND genes. This product achieves the purpose of detection by hybridizing with the CHRND 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 |
Cholinergic Receptor Nicotinic Delta Subunit |
| Gene Summary [Provided by RefSeq] |
The acetylcholine receptor of muscle has 5 subunits of 4 different types: 2 alpha and 1 each of beta, gamma and delta subunits. After acetylcholine binding, the receptor undergoes an extensive conformation change that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. Defects in this gene are a cause of multiple pterygium syndrome lethal type (MUPSL), congenital myasthenic syndrome slow-channel type (SCCMS), and congenital myasthenic syndrome fast-channel type (FCCMS). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015] |
| Gene Symbol |
CHRND |
| Location |
2q37.1 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 233390921-233400205 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-CHRND-02824-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CHRND-02824-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CHRND-02824-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CHRND-02824-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CHRND-02824-AQ |
467nm |
418nm |
|
Other Products
