Gene-specific Copy Number Variation Probe-ERCC5
Add to Cart
| Catalog: |
CNVFP-ERCC5-04685 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ERCC5). 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: |
ERCC5 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ERCC5 genes. This product achieves the purpose of detection by hybridizing with the ERCC5 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 5, Endonuclease |
| Gene Summary [Provided by RefSeq] |
This gene encodes a single-strand specific DNA endonuclease that makes the 3' incision in DNA excision repair following UV-induced damage. The protein may also function in other cellular processes, including RNA polymerase II transcription, and transcription-coupled DNA repair. Mutations in this gene cause xeroderma pigmentosum complementation group G (XP-G), which is also referred to as xeroderma pigmentosum VII (XP7), a skin disorder characterized by hypersensitivity to UV light and increased susceptibility for skin cancer development following UV exposure. Some patients also develop Cockayne syndrome, which is characterized by severe growth defects, cognitive disability, and cachexia. Read-through transcription exists between this gene and the neighboring upstream BIVM (basic, immunoglobulin-like variable motif containing) gene. [provided by RefSeq, Feb 2011] |
| Gene Symbol |
ERCC5 |
| Location |
13q33.1 |
| Chromosome |
Chromosome13 |
| Coordinates |
This gene maps to 103498190-103528351 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-ERCC5-04685-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ERCC5-04685-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ERCC5-04685-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ERCC5-04685-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ERCC5-04685-AQ |
467nm |
418nm |
|
Other Products
