Gene-specific Copy Number Variation Probe-LMOD3
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| Catalog: |
CNVFP-LMOD3-10499 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (LMOD3). 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: |
LMOD3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to LMOD3 genes. This product achieves the purpose of detection by hybridizing with the LMOD3 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 |
Leiomodin 3 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the leiomodin family of proteins. This protein contains three actin-binding domains, a tropomyosin domain, a leucine-rich repeat domain, and a Wiskott-Aldrich syndrome protein homology 2 domain (WH2). Localization of this protein to the pointed ends of thin filaments has been observed, and there is evidence that this protein acts as a catalyst of actin nucleation, and is important to the organization of sarcomeric thin filaments in skeletal muscles. Mutations in this gene have been associated as one cause of Nemaline myopathy, as other genes have also been linked to this disorder. Nemaline myopathy is a disorder characterized by nonprogressive generalized muscle weakness and protein inclusions (nemaline bodies) in skeletal myofibers. Patients with mutations in this gene often present with a severe congenital form of the disorder. [provided by RefSeq, Jan 2015] |
| Gene Symbol |
LMOD3 |
| Location |
3p14.1 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 69156038-69171746 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-LMOD3-10499-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-LMOD3-10499-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-LMOD3-10499-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-LMOD3-10499-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-LMOD3-10499-AQ |
467nm |
418nm |
|
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