Gene-specific Copy Number Variation Probe-CACNA1H
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| Catalog: |
CNVFP-CACNA1H-01848 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CACNA1H). 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: |
CACNA1H Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CACNA1H genes. This product achieves the purpose of detection by hybridizing with the CACNA1H 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 |
Calcium Voltage-gated Channel Subunit Alpha1 H |
| Gene Summary [Provided by RefSeq] |
This gene encodes a T-type member of the alpha-1 subunit family, a protein in the voltage-dependent calcium channel complex. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization and consist of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. The alpha-1 subunit has 24 transmembrane segments and forms the pore through which ions pass into the cell. There are multiple isoforms of each of the proteins in the complex, either encoded by different genes or the result of alternative splicing of transcripts. Alternate transcriptional splice variants, encoding different isoforms, have been characterized for the gene described here. Studies suggest certain mutations in this gene lead to childhood absence epilepsy (CAE). [provided by RefSeq, Jul 2008] |
| Gene Symbol |
CACNA1H |
| Location |
16p13.3 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 1203240-1271772 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-CACNA1H-01848-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CACNA1H-01848-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CACNA1H-01848-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CACNA1H-01848-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CACNA1H-01848-AQ |
467nm |
418nm |
|
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