Gene-specific Copy Number Variation Probe-HOXD13
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| Catalog: |
CNVFP-HOXD13-07023 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HOXD13). 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: |
HOXD13 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HOXD13 genes. This product achieves the purpose of detection by hybridizing with the HOXD13 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 D13 |
| Gene Summary [Provided by RefSeq] |
This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
HOXD13 |
| Location |
2q31.1 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 176957531-176960666 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-HOXD13-07023-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HOXD13-07023-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HOXD13-07023-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HOXD13-07023-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HOXD13-07023-AQ |
467nm |
418nm |
|
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