Gene-specific Copy Number Variation Probe-HOXD10
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| Catalog: |
CNVFP-HOXD10-06987 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HOXD10). 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: |
HOXD10 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HOXD10 genes. This product achieves the purpose of detection by hybridizing with the HOXD10 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 |
Homeobox D10 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the Abd-B homeobox family and encodes a protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox D genes located on chromosome 2. The encoded nuclear protein functions as a sequence-specific transcription factor that is expressed in the developing limb buds and is involved in differentiation and limb development. Mutations in this gene have been associated with Wilm's tumor and congenital vertical talus (also known as "rocker-bottom foot" deformity or congenital convex pes valgus) and/or a foot deformity resembling that seen in Charcot-Marie-Tooth disease. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
HOXD10 |
| Location |
2q31.1 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 176981491-176984670 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-HOXD10-06987-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HOXD10-06987-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HOXD10-06987-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HOXD10-06987-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HOXD10-06987-AQ |
467nm |
418nm |
|
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