Gene-specific Copy Number Variation Probe-ACSL4
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| Catalog: |
CNVFP-ACSL4-00048 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ACSL4). 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: |
ACSL4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ACSL4 genes. This product achieves the purpose of detection by hybridizing with the ACSL4 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 |
Acyl-CoA Synthetase Long Chain Family Member 4 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the cognitive disability or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants. [provided by RefSeq, Jan 2016] |
| Gene Symbol |
ACSL4 |
| Location |
Xq23 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 108884563-108976621 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-ACSL4-00048-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ACSL4-00048-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ACSL4-00048-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ACSL4-00048-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ACSL4-00048-AQ |
467nm |
418nm |
|
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