Gene-specific Copy Number Variation Probe-DDHD1
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| Catalog: |
CNVFP-DDHD1-03538 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (DDHD1). 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: |
DDHD1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to DDHD1 genes. This product achieves the purpose of detection by hybridizing with the DDHD1 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 |
DDHD Domain Containing 1 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the intracellular phospholipase A1 gene family. The protein encoded by this gene preferentially hydrolyzes phosphatidic acid. It is a cytosolic protein with some mitochondrial localization, and is thought to be involved in the regulation of mitochondrial dynamics. Overexpression of this gene causes fragmentation of the tubular structures in mitochondria, while depletion of the gene results in mitochondrial tubule elongation. Deletion of this gene in male mice caused fertility defects, resulting from disruption in the organization of the mitochondria during spermiogenesis. In humans, mutations in this gene have been associated with hereditary spastic paraplegia (HSP), also known as Strumpell-Lorrain disease, or, familial spastic paraparesis (FSP). This inherited disorder is characterized by progressive weakness and spasticity of the legs. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015] |
| Gene Symbol |
DDHD1 |
| Location |
14q22.1 |
| Chromosome |
Chromosome14 |
| Coordinates |
This gene maps to 53503457-53620046 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-DDHD1-03538-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-DDHD1-03538-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-DDHD1-03538-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-DDHD1-03538-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-DDHD1-03538-AQ |
467nm |
418nm |
|
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