Gene-specific Copy Number Variation Probe-FBLN5
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| Catalog: |
CNVFP-FBLN5-05345 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FBLN5). 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: |
FBLN5 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FBLN5 genes. This product achieves the purpose of detection by hybridizing with the FBLN5 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 |
Fibulin 5 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a secreted, extracellular matrix protein containing an Arg-Gly-Asp (RGD) motif and calcium-binding EGF-like domains. It promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. It is prominently expressed in developing arteries but less so in adult vessels. However, its expression is reinduced in balloon-injured vessels and atherosclerotic lesions, notably in intimal vascular smooth muscle cells and endothelial cells. Therefore, the protein encoded by this gene may play a role in vascular development and remodeling. Defects in this gene are a cause of autosomal dominant cutis laxa, autosomal recessive cutis laxa type I (CL type I), and age-related macular degeneration type 3 (ARMD3). [provided by RefSeq, Jul 2008] |
| Gene Symbol |
FBLN5 |
| Location |
14q32.12 |
| Chromosome |
Chromosome14 |
| Coordinates |
This gene maps to 92335754-92414046 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-FBLN5-05345-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FBLN5-05345-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FBLN5-05345-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FBLN5-05345-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FBLN5-05345-AQ |
467nm |
418nm |
|
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