Gene-specific Copy Number Variation Probe-CLDN11
Add to Cart
| Catalog: |
CNVFP-CLDN11-02767 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CLDN11). 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: |
CLDN11 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CLDN11 genes. This product achieves the purpose of detection by hybridizing with the CLDN11 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 11 |
| 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. The protein encoded by this gene is a major component of central nervous system (CNS) myelin and plays an important role in regulating proliferation and migration of oligodendrocytes. Mouse studies showed that the gene deficiency results in deafness and loss of the Sertoli cell epithelial phenotype in the testis. This protein is a tight junction protein at the human blood-testis barrier (BTB), and the BTB disruption is related to a dysfunction of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Aug 2010] |
| Gene Symbol |
CLDN11 |
| Location |
3q26.2 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 170136652-170152479 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-CLDN11-02767-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CLDN11-02767-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CLDN11-02767-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CLDN11-02767-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CLDN11-02767-AQ |
467nm |
418nm |
|
Other Products
