Gene-specific Copy Number Variation Probe-COIL
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Catalog: |
CNVFP-COIL-02896 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (COIL). 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: |
COIL Gene-specific copy number variation probes are mainly used to detect the copy number variation related to COIL genes. This product achieves the purpose of detection by hybridizing with the COIL 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 |
Coilin |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is an integral component of Cajal bodies (also called coiled bodies). Cajal bodies are nuclear suborganelles of varying number and composition that are involved in the post-transcriptional modification of small nuclear and small nucleolar RNAs. The N-terminus of the coilin protein directs its self-oligomerization while the C-terminus influences the number of nuclear bodies assembled per cell. Differential methylation and phosphorylation of coilin likely influences its localization among nuclear bodies and the composition and assembly of Cajal bodies. This gene has pseudogenes on chromosome 4 and chromosome 14. [provided by RefSeq, Jul 2008] |
Gene Symbol |
COIL |
Location |
17q22 |
Chromosome |
Chromosome17 |
Coordinates |
This gene maps to 55015560-55038411 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-COIL-02896-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-COIL-02896-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-COIL-02896-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-COIL-02896-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-COIL-02896-AQ |
467nm |
418nm |
|
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