Gene-specific Copy Number Variation Probe-BSX
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| Catalog: |
CNVFP-BSX-01517 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BSX). 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: |
BSX Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BSX genes. This product achieves the purpose of detection by hybridizing with the BSX 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 |
Brain Specific Homeobox |
| Gene Summary [Provided by RefSeq] |
The Brain Specific Homeobox (BSX) gene is located on chr11:122848356 -122852379 at 11q24.1. |
| Gene Symbol |
BSX |
| Location |
11q24.1 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 122848356-122852379 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-BSX-01517-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-BSX-01517-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-BSX-01517-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-BSX-01517-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-BSX-01517-AQ |
467nm |
418nm |
|
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