Gene-specific Copy Number Variation Probe-MYO7A
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| Catalog: |
CNVFP-MYO7A-13655 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MYO7A). 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: |
MYO7A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MYO7A genes. This product achieves the purpose of detection by hybridizing with the MYO7A 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 VIIA |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
MYO7A |
| Location |
11q13.5 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 76839309-76926286 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-MYO7A-13655-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-MYO7A-13655-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-MYO7A-13655-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-MYO7A-13655-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-MYO7A-13655-AQ |
467nm |
418nm |
|
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