Gene-specific Copy Number Variation Probe-AUH
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| Catalog: |
CNVFP-AUH-01176 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (AUH). 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: |
AUH Gene-specific copy number variation probes are mainly used to detect the copy number variation related to AUH genes. This product achieves the purpose of detection by hybridizing with the AUH 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 |
AU RNA Binding Methylglutaconyl-CoA Hydratase |
| Gene Summary [Provided by RefSeq] |
This gene encodes bifunctional mitochondrial protein that has both RNA-binding and hydratase activities. The encoded protein is a methylglutaconyl-CoA hydratase that catalyzes the hydration of 3-methylglutaconyl-CoA to 3-hydroxy-3-methyl-glutaryl-CoA, a critical step in the leucine degradation pathway. This protein also binds AU-rich elements (AREs) found in the 3' UTRs of rapidly decaying mRNAs including c-fos, c-myc and granulocyte/ macrophage colony stimulating factor. ARE elements are involved in directing RNA to rapid degradation and deadenylation. This protein is localizes to the mitochondrial matrix and the inner mitochondrial membrane and may be involved in mitochondrial protein synthesis. Mutations in this gene are the cause of 3-methylglutaconic aciduria, type I. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015] |
| Gene Symbol |
AUH |
| Location |
9q22.31 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 93976096-94124206 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-AUH-01176-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-AUH-01176-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-AUH-01176-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-AUH-01176-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-AUH-01176-AQ |
467nm |
418nm |
|
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