Gene-specific Copy Number Variation Probe-COCH
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| Catalog: |
CNVFP-COCH-02869 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (COCH). 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: |
COCH Gene-specific copy number variation probes are mainly used to detect the copy number variation related to COCH genes. This product achieves the purpose of detection by hybridizing with the COCH 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 |
Cochlin |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is highly conserved in human, mouse, and chicken, showing 94% and 79% amino acid identity of human to mouse and chicken sequences, respectively. Hybridization to this gene was detected in spindle-shaped cells located along nerve fibers between the auditory ganglion and sensory epithelium. These cells accompany neurites at the habenula perforata, the opening through which neurites extend to innervate hair cells. This and the pattern of expression of this gene in chicken inner ear paralleled the histologic findings of acidophilic deposits, consistent with mucopolysaccharide ground substance, in temporal bones from DFNA9 (autosomal dominant nonsyndromic sensorineural deafness 9) patients. Mutations that cause DFNA9 have been reported in this gene. Alternative splicing results in multiple transcript variants encoding the same protein. Additional splice variants encoding distinct isoforms have been described but their biological validities have not been demonstrated. [provided by RefSeq, Oct 2008] |
| Gene Symbol |
COCH |
| Location |
14q12 |
| Chromosome |
Chromosome14 |
| Coordinates |
This gene maps to 31343740-31359822 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-COCH-02869-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-COCH-02869-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-COCH-02869-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-COCH-02869-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-COCH-02869-AQ |
467nm |
418nm |
|
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