Gene-specific Copy Number Variation Probe-CSE1L
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| Catalog: |
CNVFP-CSE1L-03273 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CSE1L). 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: |
CSE1L Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CSE1L genes. This product achieves the purpose of detection by hybridizing with the CSE1L 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 |
Chromosome Segregation 1 Like |
| Gene Summary [Provided by RefSeq] |
Proteins that carry a nuclear localization signal (NLS) are transported into the nucleus by the importin-alpha/beta heterodimer. Importin-alpha binds the NLS, while importin-beta mediates translocation through the nuclear pore complex. After translocation, RanGTP binds importin-beta and displaces importin-alpha. Importin-alpha must then be returned to the cytoplasm, leaving the NLS protein behind. The protein encoded by this gene binds strongly to NLS-free importin-alpha, and this binding is released in the cytoplasm by the combined action of RANBP1 and RANGAP1. In addition, the encoded protein may play a role both in apoptosis and in cell proliferation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012] |
| Gene Symbol |
CSE1L |
| Location |
20q13.13 |
| Chromosome |
Chromosome20 |
| Coordinates |
This gene maps to 47662837-47713486 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-CSE1L-03273-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CSE1L-03273-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CSE1L-03273-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CSE1L-03273-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CSE1L-03273-AQ |
467nm |
418nm |
|
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