Gene-specific Copy Number Variation Probe-FBN1
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| Catalog: |
CNVFP-FBN1-05344 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FBN1). 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: |
FBN1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FBN1 genes. This product achieves the purpose of detection by hybridizing with the FBN1 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 |
Fibrillin 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the fibrillin family of proteins. The encoded preproprotein is proteolytically processed to generate two proteins including the extracellular matrix component fibrillin-1 and the protein hormone asprosin. Fibrillin-1 is an extracellular matrix glycoprotein that serves as a structural component of calcium-binding microfibrils. These microfibrils provide force-bearing structural support in elastic and nonelastic connective tissue throughout the body. Asprosin, secreted by white adipose tissue, has been shown to regulate glucose homeostasis. Mutations in this gene are associated with Marfan syndrome and the related MASS phenotype, as well as ectopia lentis syndrome, Weill-Marchesani syndrome, Shprintzen-Goldberg syndrome and neonatal progeroid syndrome. [provided by RefSeq, Apr 2016] |
| Gene Symbol |
FBN1 |
| Location |
15q21.1 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 48700502-48937985 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-FBN1-05344-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FBN1-05344-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FBN1-05344-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FBN1-05344-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FBN1-05344-AQ |
467nm |
418nm |
|
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