Gene-specific Copy Number Variation Probe-FBL
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| Catalog: |
CNVFP-FBL-05349 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FBL). 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: |
FBL Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FBL genes. This product achieves the purpose of detection by hybridizing with the FBL 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 |
Fibrillarin |
| Gene Summary [Provided by RefSeq] |
This gene product is a component of a nucleolar small nuclear ribonucleoprotein (snRNP) particle thought to participate in the first step in processing preribosomal RNA. It is associated with the U3, U8, and U13 small nuclear RNAs and is located in the dense fibrillar component (DFC) of the nucleolus. The encoded protein contains an N-terminal repetitive domain that is rich in glycine and arginine residues, like fibrillarins in other species. Its central region resembles an RNA-binding domain and contains an RNP consensus sequence. Antisera from approximately 8% of humans with the autoimmune disease scleroderma recognize fibrillarin. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
FBL |
| Location |
19q13.2 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 40325092-40337054 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-FBL-05349-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FBL-05349-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FBL-05349-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FBL-05349-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FBL-05349-AQ |
467nm |
418nm |
|
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