Gene-specific Copy Number Variation Probe-ACTG1
Add to Cart
| Catalog: |
CNVFP-ACTG1-00124 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ACTG1). 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: |
ACTG1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ACTG1 genes. This product achieves the purpose of detection by hybridizing with the ACTG1 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 Gamma 1 |
| Gene Summary [Provided by RefSeq] |
Actins are highly conserved proteins that are involved in various types of cell motility and in maintenance of the cytoskeleton. Three main groups of actin isoforms have been identified in vertebrate animals: alpha, beta, and gamma. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. The beta and gamma actins co-exist in most cell types as components of the cytoskeleton and as mediators of internal cell motility. Actin gamma 1, encoded by this gene, is a cytoplasmic actin found in all cell types. Mutations in this gene are associated with DFNA20/26, a subtype of autosomal dominant non-syndromic sensorineural progressive hearing loss and also with Baraitser-Winter syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017] |
| Gene Symbol |
ACTG1 |
| Location |
17q25.3 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 79476996-79479892 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-ACTG1-00124-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ACTG1-00124-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ACTG1-00124-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ACTG1-00124-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ACTG1-00124-AQ |
467nm |
418nm |
|
Other Products
