Gene-specific Copy Number Variation Probe-JAM3
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| Catalog: |
CNVFP-JAM3-07896 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (JAM3). 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: |
JAM3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to JAM3 genes. This product achieves the purpose of detection by hybridizing with the JAM3 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 |
Junctional Adhesion Molecule 3 |
| 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. The protein encoded by this immunoglobulin superfamily gene member is localized in the tight junctions between high endothelial cells. Unlike other proteins in this family, the this protein is unable to adhere to leukocyte cell lines and only forms weak homotypic interactions. The encoded protein is a member of the junctional adhesion molecule protein family and acts as a receptor for another member of this family. A mutation in an intron of this gene is associated with hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Apr 2011] |
| Gene Symbol |
JAM3 |
| Location |
11q25 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 133938819-134021652 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-JAM3-07896-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-JAM3-07896-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-JAM3-07896-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-JAM3-07896-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-JAM3-07896-AQ |
467nm |
418nm |
|
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