Gene-specific Copy Number Variation Probe-TPM1
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| Catalog: |
CNVFP-TPM1-21476 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TPM1). 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: |
TPM1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TPM1 genes. This product achieves the purpose of detection by hybridizing with the TPM1 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 |
Tropomyosin 1 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the tropomyosin family of highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosin is composed of two alpha-helical chains arranged as a coiled-coil. It is polymerized end to end along the two grooves of actin filaments and provides stability to the filaments. The encoded protein is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle, where it also functions in association with the troponin complex to regulate the calcium-dependent interaction of actin and myosin during muscle contraction. In smooth muscle and non-muscle cells, alternatively spliced transcript variants encoding a range of isoforms have been described. Mutations in this gene are associated with type 3 familial hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
TPM1 |
| Location |
15q22.2 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 63334837-63364113 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-TPM1-21476-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TPM1-21476-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TPM1-21476-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TPM1-21476-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TPM1-21476-AQ |
467nm |
418nm |
|
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