Gene-specific Copy Number Variation Probe-DLX3
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| Catalog: |
CNVFP-DLX3-03942 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (DLX3). 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: |
DLX3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to DLX3 genes. This product achieves the purpose of detection by hybridizing with the DLX3 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 |
Distal-less Homeobox 3 |
| Gene Summary [Provided by RefSeq] |
Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
DLX3 |
| Location |
17q21.33 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 48067368-48072588 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-DLX3-03942-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-DLX3-03942-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-DLX3-03942-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-DLX3-03942-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-DLX3-03942-AQ |
467nm |
418nm |
|
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