Gene-specific Copy Number Variation Probe-HOXA13
Add to Cart
| Catalog: |
CNVFP-HOXA13-07037 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HOXA13). 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: |
HOXA13 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HOXA13 genes. This product achieves the purpose of detection by hybridizing with the HOXA13 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 A13 |
| Gene Summary [Provided by RefSeq] |
In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. Expansion of a polyalanine tract in the encoded protein can cause hand-foot-uterus syndrome, also known as hand-foot-genital syndrome. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
HOXA13 |
| Location |
7p15.2 |
| Chromosome |
Chromosome7 |
| Coordinates |
This gene maps to 27236498-27239725 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-HOXA13-07037-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HOXA13-07037-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HOXA13-07037-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HOXA13-07037-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HOXA13-07037-AQ |
467nm |
418nm |
|
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