Gene-specific Copy Number Variation Probe-RNASEH1
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| Catalog: |
CNVFP-RNASEH1-17324 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RNASEH1). 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: |
RNASEH1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RNASEH1 genes. This product achieves the purpose of detection by hybridizing with the RNASEH1 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 |
Ribonuclease H1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes an endonuclease that specifically degrades the RNA of RNA-DNA hybrids and plays a key role in DNA replication and repair. Alternate in-frame start codon initiation results in the production of alternate isoforms that are directed to the mitochondria or to the nucleus. The production of the mitochondrial isoform is modulated by an upstream open reading frame (uORF). Mutations in this gene have been found in individuals with progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2. Alternative splicing results in additional coding and non-coding transcript variants. Pseudogenes of this gene have been defined on chromosomes 2 and 17. [provided by RefSeq, Jul 2017] |
| Gene Symbol |
RNASEH1 |
| Location |
2p25.3 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 3592690-3605940 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-RNASEH1-17324-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RNASEH1-17324-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RNASEH1-17324-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RNASEH1-17324-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RNASEH1-17324-AQ |
467nm |
418nm |
|
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