Gene-specific Copy Number Variation Probe-HSD17B10
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| Catalog: |
CNVFP-HSD17B10-06921 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HSD17B10). 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: |
HSD17B10 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HSD17B10 genes. This product achieves the purpose of detection by hybridizing with the HSD17B10 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 |
Hydroxysteroid 17-beta Dehydrogenase 10 |
| Gene Summary [Provided by RefSeq] |
This gene encodes 3-hydroxyacyl-CoA dehydrogenase type II, a member of the short-chain dehydrogenase/reductase superfamily. The gene product is a mitochondrial protein that catalyzes the oxidation of a wide variety of fatty acids and steroids, and is a subunit of mitochondrial ribonuclease P, which is involved in tRNA maturation. The protein has been implicated in the development of Alzheimer disease, and mutations in the gene are the cause of 17beta-hydroxysteroid dehydrogenase type 10 (HSD10) deficiency. Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Aug 2014] |
| Gene Symbol |
HSD17B10 |
| Location |
Xp11.22 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 53458205-53461323 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-HSD17B10-06921-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HSD17B10-06921-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HSD17B10-06921-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HSD17B10-06921-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HSD17B10-06921-AQ |
467nm |
418nm |
|
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