Gene-specific Copy Number Variation Probe-CYP7B1
Add to Cart
| Catalog: |
CNVFP-CYP7B1-03666 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CYP7B1). 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: |
CYP7B1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CYP7B1 genes. This product achieves the purpose of detection by hybridizing with the CYP7B1 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 |
Cytochrome P450 Family 7 Subfamily B Member 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum membrane protein catalyzes the first reaction in the cholesterol catabolic pathway of extrahepatic tissues, which converts cholesterol to bile acids. This enzyme likely plays a minor role in total bile acid synthesis, but may also be involved in the development of atherosclerosis, neurosteroid metabolism and sex hormone synthesis. Mutations in this gene have been associated with hereditary spastic paraplegia (SPG5 or HSP), an autosomal recessive disorder. [provided by RefSeq, Apr 2016] |
| Gene Symbol |
CYP7B1 |
| Location |
8q12.3 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 65508528-65711348 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-CYP7B1-03666-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CYP7B1-03666-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CYP7B1-03666-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CYP7B1-03666-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CYP7B1-03666-AQ |
467nm |
418nm |
|
Other Products
