Gene-specific Copy Number Variation Probe-MYH9
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| Catalog: |
CNVFP-MYH9-13726 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MYH9). 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: |
MYH9 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MYH9 genes. This product achieves the purpose of detection by hybridizing with the MYH9 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 Heavy Chain 9 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011] |
| Gene Symbol |
MYH9 |
| Location |
22q12.3 |
| Chromosome |
Chromosome22 |
| Coordinates |
This gene maps to 36677322-36784063 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-MYH9-13726-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-MYH9-13726-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-MYH9-13726-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-MYH9-13726-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-MYH9-13726-AQ |
467nm |
418nm |
|
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