Gene-specific Copy Number Variation Probe-ACTA1
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| Catalog: |
CNVFP-ACTA1-00130 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ACTA1). 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: |
ACTA1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ACTA1 genes. This product achieves the purpose of detection by hybridizing with the ACTA1 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 |
Actin, Alpha 1, Skeletal Muscle |
| Gene Summary [Provided by RefSeq] |
The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
ACTA1 |
| Location |
1q42.13 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 229566992-229569843 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-ACTA1-00130-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ACTA1-00130-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ACTA1-00130-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ACTA1-00130-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ACTA1-00130-AQ |
467nm |
418nm |
|
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