Gene-specific Copy Number Variation Probe-MYO3A
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| Catalog: |
CNVFP-MYO3A-13660 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MYO3A). 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: |
MYO3A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MYO3A genes. This product achieves the purpose of detection by hybridizing with the MYO3A 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 |
Myosin IIIA |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene belongs to the myosin superfamily. Myosins are actin-dependent motor proteins and are categorized into conventional myosins (class II) and unconventional myosins (classes I and III through XV) based on their variable C-terminal cargo-binding domains. Class III myosins, such as this one, have a kinase domain N-terminal to the conserved N-terminal motor domains and are expressed in photoreceptors. The protein encoded by this gene plays an important role in hearing in humans. Three different recessive, loss of function mutations in the encoded protein have been shown to cause nonsyndromic progressive hearing loss. Expression of this gene is highly restricted, with the strongest expression in retina and cochlea. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
MYO3A |
| Location |
10p12.1 |
| Chromosome |
Chromosome10 |
| Coordinates |
This gene maps to 26223001-26501465 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-MYO3A-13660-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-MYO3A-13660-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-MYO3A-13660-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-MYO3A-13660-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-MYO3A-13660-AQ |
467nm |
418nm |
|
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