Gene-specific Copy Number Variation Probe-HARS2
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| Catalog: |
CNVFP-HARS2-06679 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HARS2). 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: |
HARS2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HARS2 genes. This product achieves the purpose of detection by hybridizing with the HARS2 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 |
Histidyl-tRNA Synthetase 2, Mitochondrial |
| Gene Summary [Provided by RefSeq] |
Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. The protein encoded by this gene is an enzyme belonging to the class II family of aminoacyl-tRNA synthetases. Functioning in the synthesis of histidyl-transfer RNA, the enzyme plays an accessory role in the regulation of protein biosynthesis. The gene is located in a head-to-head orientation with HARS on chromosome five, where the homologous genes likely share a bidirectional promoter. Mutations in this gene are associated with the pathogenesis of Perrault syndrome, which involves ovarian dysgenesis and sensorineural hearing loss. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013] |
| Gene Symbol |
HARS2 |
| Location |
5q31.3 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 140071017-140078890 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-HARS2-06679-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HARS2-06679-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HARS2-06679-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HARS2-06679-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HARS2-06679-AQ |
467nm |
418nm |
|
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