Gene-specific Copy Number Variation Probe-HSD11B1
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| Catalog: |
CNVFP-HSD11B1-06929 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HSD11B1). 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: |
HSD11B1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HSD11B1 genes. This product achieves the purpose of detection by hybridizing with the HSD11B1 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 |
Hydroxysteroid 11-beta Dehydrogenase 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a microsomal enzyme that catalyzes the conversion of the stress hormone cortisol to the inactive metabolite cortisone. In addition, the encoded protein can catalyze the reverse reaction, the conversion of cortisone to cortisol. Too much cortisol can lead to central obesity, and a particular variation in this gene has been associated with obesity and insulin resistance in children. Mutations in this gene and H6PD (hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)) are the cause of cortisone reductase deficiency. Alternate splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq, May 2011] |
| Gene Symbol |
HSD11B1 |
| Location |
1q32.2 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 209859524-209908295 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-HSD11B1-06929-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HSD11B1-06929-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HSD11B1-06929-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HSD11B1-06929-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HSD11B1-06929-AQ |
467nm |
418nm |
|
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