Gene-specific Copy Number Variation Probe-CLDN1
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Catalog: |
CNVFP-CLDN1-02768 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CLDN1). 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: |
CLDN1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CLDN1 genes. This product achieves the purpose of detection by hybridizing with the CLDN1 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 1 |
Gene Summary [Provided by RefSeq] |
Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. Loss of function mutations result in neonatal ichthyosis-sclerosing cholangitis syndrome. [provided by RefSeq, Jul 2008] |
Gene Symbol |
CLDN1 |
Location |
3q28 |
Chromosome |
Chromosome3 |
Coordinates |
This gene maps to 190023489-190040235 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-CLDN1-02768-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-CLDN1-02768-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-CLDN1-02768-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-CLDN1-02768-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-CLDN1-02768-AQ |
467nm |
418nm |
|
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