Gene-specific Copy Number Variation Probe-ERCC2
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| Catalog: |
CNVFP-ERCC2-04688 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ERCC2). 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: |
ERCC2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ERCC2 genes. This product achieves the purpose of detection by hybridizing with the ERCC2 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 2, TFIIH Core Complex Helicase Subunit |
| Gene Summary [Provided by RefSeq] |
The nucleotide excision repair pathway is a mechanism to repair damage to DNA. The protein encoded by this gene is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. The gene product has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in this gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008] |
| Gene Symbol |
ERCC2 |
| Location |
19q13.32 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 45854648-45873845 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-ERCC2-04688-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ERCC2-04688-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ERCC2-04688-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ERCC2-04688-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ERCC2-04688-AQ |
467nm |
418nm |
|
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