Gene-specific Copy Number Variation Probe-HSD3B7
Add to Cart
| Catalog: |
CNVFP-HSD3B7-06950 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HSD3B7). 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: |
HSD3B7 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HSD3B7 genes. This product achieves the purpose of detection by hybridizing with the HSD3B7 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 |
Hydroxy-delta-5-steroid Dehydrogenase, 3 Beta- And Steroid Delta-isomerase 7 |
| Gene Summary [Provided by RefSeq] |
This gene encodes an enzyme which is involved in the initial stages of the synthesis of bile acids from cholesterol and a member of the short-chain dehydrogenase/reductase superfamily. The encoded protein is a membrane-associated endoplasmic reticulum protein which is active against 7-alpha hydrosylated sterol substrates. Mutations in this gene are associated with a congenital bile acid synthesis defect which leads to neonatal cholestasis, a form of progressive liver disease. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008] |
| Gene Symbol |
HSD3B7 |
| Location |
16p11.2 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 30996518-31000473 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-HSD3B7-06950-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HSD3B7-06950-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HSD3B7-06950-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HSD3B7-06950-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HSD3B7-06950-AQ |
467nm |
418nm |
|
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