Gene-specific Copy Number Variation Probe-CLN8
Add to Cart
| Catalog: |
CNVFP-CLN8-02966 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CLN8). 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: |
CLN8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CLN8 genes. This product achieves the purpose of detection by hybridizing with the CLN8 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 |
CLN8, Transmembrane ER And ERGIC Protein |
| Gene Summary [Provided by RefSeq] |
This gene encodes a transmembrane protein belonging to a family of proteins containing TLC domains, which are postulated to function in lipid synthesis, transport, or sensing. The protein localizes to the endoplasmic reticulum (ER), and may recycle between the ER and ER-Golgi intermediate compartment. Mutations in this gene are associated with a disorder characterized by progressive epilepsy with cognitive disabilities (EPMR), which is a subtype of neuronal ceroid lipofuscinoses (NCL). Patients with mutations in this gene have altered levels of sphingolipid and phospholipids in the brain. [provided by RefSeq, Jul 2017] |
| Gene Symbol |
CLN8 |
| Location |
8p23.3 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 1711869-1734736 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-CLN8-02966-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CLN8-02966-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CLN8-02966-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CLN8-02966-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CLN8-02966-AQ |
467nm |
418nm |
|
Other Products
