Gene-specific Copy Number Variation Probe-DYM
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| Catalog: |
CNVFP-DYM-04206 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (DYM). 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: |
DYM Gene-specific copy number variation probes are mainly used to detect the copy number variation related to DYM genes. This product achieves the purpose of detection by hybridizing with the DYM 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 |
Dymeclin |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein which regulates Golgi-associated secretory pathways that are essential to endochondral bone formation during early development. This gene is also believed to play a role in early brain development. This gene is widely expressed in embryos and is particularly abundant in chodrocytes and brain tissues. It encodes a peripheral membrane protein which shuttles between the cytosol and Golgi complex. Mutations in this gene are associated with two types of recessive osteochondrodysplasia: Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia. [provided by RefSeq, Jun 2017] |
| Gene Symbol |
DYM |
| Location |
18q21.1 |
| Chromosome |
Chromosome18 |
| Coordinates |
This gene maps to 46570171-46987079 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-DYM-04206-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-DYM-04206-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-DYM-04206-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-DYM-04206-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-DYM-04206-AQ |
467nm |
418nm |
|
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