Gene-specific Copy Number Variation Probe-CLDN9
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| Catalog: |
CNVFP-CLDN9-02747 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CLDN9). 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: |
CLDN9 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CLDN9 genes. This product achieves the purpose of detection by hybridizing with the CLDN9 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 |
Claudin 9 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This protein is one of the entry cofactors for hepatitis C virus. Mouse studies revealed that this gene is required for the preservation of sensory cells in the hearing organ and the gene deficiency is associated with deafness. [provided by RefSeq, Jun 2010] |
| Gene Symbol |
CLDN9 |
| Location |
16p13.3 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 3062456-3064506 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-CLDN9-02747-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CLDN9-02747-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CLDN9-02747-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CLDN9-02747-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CLDN9-02747-AQ |
467nm |
418nm |
|
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