Gene-specific Copy Number Variation Probe-SLC25A20
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| Catalog: |
CNVFP-SLC25A20-18554 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC25A20). 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: |
SLC25A20 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC25A20 genes. This product achieves the purpose of detection by hybridizing with the SLC25A20 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 |
Solute Carrier Family 25 Member 20 |
| Gene Summary [Provided by RefSeq] |
This gene product is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. This protein mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
SLC25A20 |
| Location |
3p21.31 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 48894355-48936426 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-SLC25A20-18554-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SLC25A20-18554-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SLC25A20-18554-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SLC25A20-18554-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SLC25A20-18554-AQ |
467nm |
418nm |
|
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