Gene-specific Copy Number Variation Probe-SYNE4
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| Catalog: |
CNVFP-SYNE4-20250 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SYNE4). 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: |
SYNE4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SYNE4 genes. This product achieves the purpose of detection by hybridizing with the SYNE4 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 |
Spectrin Repeat Containing Nuclear Envelope Family Member 4 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the nesprin family of genes, that encode KASH (Klarsicht, Anc-1, Syne Homology) domain-containing proteins. In addition to the KASH domain, this protein also contains a coiled-coil and leucine zipper region, a spectrin repeat, and a kinesin-1 binding region. This protein localizes to the outer nuclear membrane, and is part of the linker of nucleoskeleton and cytoskeleton (LINC) complex in the nuclear envelope. LINC complexes are formed by SUN (Sad1, UNC-84)-KASH pairs, and are thought to mechanically couple nuclear components to the cytoskeleton. Mutations in this gene have been associated with progressive high-frequency hearing loss. The absence of this protein in mice also caused hearing loss, and changes in hair cell morphology in the ears. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015] |
| Gene Symbol |
SYNE4 |
| Location |
19q13.12 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 36008792-36003298 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-SYNE4-20250-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SYNE4-20250-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SYNE4-20250-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SYNE4-20250-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SYNE4-20250-AQ |
467nm |
418nm |
|
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