Gene-specific Copy Number Variation Probe-FCN3
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| Catalog: |
CNVFP-FCN3-05282 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FCN3). 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: |
FCN3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FCN3 genes. This product achieves the purpose of detection by hybridizing with the FCN3 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 |
Ficolin 3 |
| Gene Summary [Provided by RefSeq] |
Ficolins are a group of proteins which consist of a collagen-like domain and a fibrinogen-like domain. In human serum, there are two types of ficolins, both of which have lectin activity. The protein encoded by this gene is a thermolabile beta-2-macroglycoprotein found in all human serum and is a member of the ficolin/opsonin p35 lectin family. The protein, which was initially identified based on its reactivity with sera from patients with systemic lupus erythematosus, has been shown to have a calcium-independent lectin activity. The protein can activate the complement pathway in association with MASPs and sMAP, thereby aiding in host defense through the activation of the lectin pathway. Alternative splicing occurs at this locus and two variants, each encoding a distinct isoform, have been identified. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
FCN3 |
| Location |
1p36.11 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 27695600-27701315 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-FCN3-05282-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FCN3-05282-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FCN3-05282-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FCN3-05282-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FCN3-05282-AQ |
467nm |
418nm |
|
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