Gene-specific Copy Number Variation Probe-TNNT1
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| Catalog: |
CNVFP-TNNT1-21163 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TNNT1). 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: |
TNNT1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TNNT1 genes. This product achieves the purpose of detection by hybridizing with the TNNT1 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 |
Troponin T1, Slow Skeletal Type |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
TNNT1 |
| Location |
19q13.42 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 55644160-55660606 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-TNNT1-21163-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TNNT1-21163-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TNNT1-21163-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TNNT1-21163-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TNNT1-21163-AQ |
467nm |
418nm |
|
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