Gene-specific Copy Number Variation Probe-RNASEH2A
Add to Cart
| Catalog: |
CNVFP-RNASEH2A-17323 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RNASEH2A). 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: |
RNASEH2A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RNASEH2A genes. This product achieves the purpose of detection by hybridizing with the RNASEH2A 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 H2 Subunit A |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a component of the heterotrimeric type II ribonuclease H enzyme (RNAseH2). RNAseH2 is the major source of ribonuclease H activity in mammalian cells and endonucleolytically cleaves ribonucleotides. It is predicted to remove Okazaki fragment RNA primers during lagging strand DNA synthesis and to excise single ribonucleotides from DNA-DNA duplexes. Mutations in this gene cause Aicardi-Goutieres Syndrome (AGS), a an autosomal recessive neurological disorder characterized by progressive microcephaly and psychomotor retardation, intracranial calcifications, elevated levels of interferon-alpha and white blood cells in the cerebrospinal fluid.[provided by RefSeq, Aug 2009] |
| Gene Symbol |
RNASEH2A |
| Location |
19p13.13 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 12917427-12924462 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-RNASEH2A-17323-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RNASEH2A-17323-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RNASEH2A-17323-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RNASEH2A-17323-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RNASEH2A-17323-AQ |
467nm |
418nm |
|
Other Products
