Gene-specific Copy Number Variation Probe-TRPM7
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| Catalog: |
CNVFP-TRPM7-22141 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TRPM7). 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: |
TRPM7 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TRPM7 genes. This product achieves the purpose of detection by hybridizing with the TRPM7 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 |
Transient Receptor Potential Cation Channel Subfamily M Member 7 |
| Gene Summary [Provided by RefSeq] |
This gene belongs to the melastatin subfamily of transient receptor potential family of ion channels. The protein encoded by this gene is both an ion channel and a serine/threonine protein kinase. The kinase activity is essential for the ion channel function, which serves to increase intracellular calcium levels and to help regulate magnesium ion homeostasis. The encoded protein is involved in cytoskeletal organization, cell adhesion, cell migration and organogenesis. Defects in this gene are a cause of amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam. The gene may also be associated with defects of cardiac function. [provided by RefSeq, Aug 2017] |
| Gene Symbol |
TRPM7 |
| Location |
15q21.2 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 50849351-50979012 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-TRPM7-22141-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TRPM7-22141-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TRPM7-22141-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TRPM7-22141-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TRPM7-22141-AQ |
467nm |
418nm |
|
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