Gene-specific Copy Number Variation Probe-TRPM5
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| Catalog: |
CNVFP-TRPM5-22143 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TRPM5). 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: |
TRPM5 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TRPM5 genes. This product achieves the purpose of detection by hybridizing with the TRPM5 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 5 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the transient receptor potential (TRP) protein family, which is a diverse group of proteins with structural features typical of ion channels. This protein plays an important role in taste transduction, and has characteristics of a calcium-activated, non-selective cation channel that carries Na+, K+, and Cs+ ions equally well, but not Ca(2+) ions. It is activated by lower concentrations of intracellular Ca(2+), and inhibited by higher concentrations. It is also a highly temperature-sensitive, heat activated channel showing a steep increase of inward currents at temperatures between 15 and 35 degrees Celsius. This gene is located within the Beckwith-Wiedemann syndrome critical region-1 on chromosome 11p15.5, and has been shown to be imprinted, with exclusive expression from the paternal allele. [provided by RefSeq, Oct 2010] |
| Gene Symbol |
TRPM5 |
| Location |
11p15.5 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 2425745-2444275 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-TRPM5-22143-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TRPM5-22143-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TRPM5-22143-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TRPM5-22143-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TRPM5-22143-AQ |
467nm |
418nm |
|
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