Gene-specific Copy Number Variation Probe-HSD17B4
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| Catalog: |
CNVFP-HSD17B4-06918 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HSD17B4). 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: |
HSD17B4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HSD17B4 genes. This product achieves the purpose of detection by hybridizing with the HSD17B4 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 4 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014] |
| Gene Symbol |
HSD17B4 |
| Location |
5q23.1 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 118788137-118878030 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-HSD17B4-06918-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HSD17B4-06918-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HSD17B4-06918-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HSD17B4-06918-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HSD17B4-06918-AQ |
467nm |
418nm |
|
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