Gene-specific Copy Number Variation Probe-ERCC6L
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| Catalog: |
CNVFP-ERCC6L-04647 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ERCC6L). 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: |
ERCC6L Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ERCC6L genes. This product achieves the purpose of detection by hybridizing with the ERCC6L 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 |
ERCC Excision Repair 6 Like, Spindle Assembly Checkpoint Helicase |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the SWItch/Sucrose Non-Fermentable (SWI/SNF2) family of proteins, and contains a SNF2-like ATPase domain and a PICH family domain. One distinguishing feature of this SWI/SNF protein family member is that during interphase, the protein is excluded from the nucleus, and only associates with chromatin after the nuclear envelope has broken down. This protein is a DNA translocase that is thought to bind double-stranded DNA that is exposed to stretching forces, such as those exerted by the mitotic spindle. This protein associates with ribosomal DNA and ultra-fine DNA bridges (UFBs), fine structures that connect sister chromatids during anaphase at some sites such as fragile sites, telomeres and centromeres. This gene is required for the faithful segregation of sister chromatids during mitosis, and the ATPase activity of this protein required for the resolution of UFBs before cytokinesis. [provided by RefSeq, May 2017] |
| Gene Symbol |
ERCC6L |
| Location |
Xq13.1 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 71424506-71458858 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-ERCC6L-04647-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ERCC6L-04647-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ERCC6L-04647-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ERCC6L-04647-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ERCC6L-04647-AQ |
467nm |
418nm |
|
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