Gene-specific Copy Number Variation Probe-NEB
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| Catalog: |
CNVFP-NEB-13983 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NEB). 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: |
NEB Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NEB genes. This product achieves the purpose of detection by hybridizing with the NEB 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 |
Nebulin |
| Gene Summary [Provided by RefSeq] |
This gene encodes nebulin, a giant protein component of the cytoskeletal matrix that coexists with the thick and thin filaments within the sarcomeres of skeletal muscle. In most vertebrates, nebulin accounts for 3 to 4% of the total myofibrillar protein. The encoded protein contains approximately 30-amino acid long modules that can be classified into 7 types and other repeated modules. Protein isoform sizes vary from 600 to 800 kD due to alternative splicing that is tissue-, species-,and developmental stage-specific. Of the 183 exons in the nebulin gene, at least 43 are alternatively spliced, although exons 143 and 144 are not found in the same transcript. Of the several thousand transcript variants predicted for nebulin, the RefSeq Project has decided to create three representative RefSeq records. Mutations in this gene are associated with recessive nemaline myopathy. [provided by RefSeq, Sep 2009] |
| Gene Symbol |
NEB |
| Location |
2q23.3 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 152341852-152591001 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-NEB-13983-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NEB-13983-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NEB-13983-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NEB-13983-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NEB-13983-AQ |
467nm |
418nm |
|
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