Gene-specific Copy Number Variation Probe-LMNA
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| Catalog: |
CNVFP-LMNA-10536 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (LMNA). 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: |
LMNA Gene-specific copy number variation probes are mainly used to detect the copy number variation related to LMNA genes. This product achieves the purpose of detection by hybridizing with the LMNA 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 |
Lamin A/C |
| Gene Summary [Provided by RefSeq] |
The nuclear lamina consists of a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure and gene expression. Vertebrate lamins consist of two types, A and B. Alternative splicing results in multiple transcript variants. Mutations in this gene lead to several diseases: Emery-Dreifuss muscular dystrophy, familial partial lipodystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy, Charcot-Marie-Tooth disease, and Hutchinson-Gilford progeria syndrome. [provided by RefSeq, Apr 2012] |
| Gene Symbol |
LMNA |
| Location |
1q22 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 156084460-156109878 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-LMNA-10536-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-LMNA-10536-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-LMNA-10536-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-LMNA-10536-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-LMNA-10536-AQ |
467nm |
418nm |
|
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