Gene-specific Copy Number Variation Probe-CALM2
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| Catalog: |
CNVFP-CALM2-01827 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CALM2). 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: |
CALM2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CALM2 genes. This product achieves the purpose of detection by hybridizing with the CALM2 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 |
Calmodulin 2 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the calmodulin gene family. There are three distinct calmodulin genes dispersed throughout the genome that encode the identical protein, but differ at the nucleotide level. Calmodulin is a calcium binding protein that plays a role in signaling pathways, cell cycle progression and proliferation. Several infants with severe forms of long-QT syndrome (LQTS) who displayed life-threatening ventricular arrhythmias together with delayed neurodevelopment and epilepsy were found to have mutations in either this gene or another member of the calmodulin gene family (PMID:23388215). Mutations in this gene have also been identified in patients with less severe forms of LQTS (PMID:24917665), while mutations in another calmodulin gene family member have been associated with catecholaminergic polymorphic ventricular tachycardia (CPVT)(PMID:23040497), a rare disorder thought to be the cause of a significant fraction of sudden cardiac deaths in young individuals. Pseudogenes of this gene are found on chromosomes 10, 13, and 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015] |
| Gene Symbol |
CALM2 |
| Location |
2p21 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 47387220-47403740 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-CALM2-01827-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CALM2-01827-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CALM2-01827-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CALM2-01827-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CALM2-01827-AQ |
467nm |
418nm |
|
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