Gene-specific Copy Number Variation Probe-CLCN7
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| Catalog: |
CNVFP-CLCN7-02695 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CLCN7). 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: |
CLCN7 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CLCN7 genes. This product achieves the purpose of detection by hybridizing with the CLCN7 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 |
Chloride Voltage-gated Channel 7 |
| Gene Summary [Provided by RefSeq] |
The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
CLCN7 |
| Location |
16p13.3 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 1494934-1525085 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-CLCN7-02695-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CLCN7-02695-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CLCN7-02695-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CLCN7-02695-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CLCN7-02695-AQ |
467nm |
418nm |
|
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