Gene-specific Copy Number Variation Probe-CYP21A2
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| Catalog: |
CNVFP-CYP21A2-03383 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CYP21A2). 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: |
CYP21A2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CYP21A2 genes. This product achieves the purpose of detection by hybridizing with the CYP21A2 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 21 Subfamily A Member 2 |
| 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 protein localizes to the endoplasmic reticulum and hydroxylates steroids at the 21 position. Its activity is required for the synthesis of steroid hormones including cortisol and aldosterone. Mutations in this gene cause congenital adrenal hyperplasia. A related pseudogene is located near this gene; gene conversion events involving the functional gene and the pseudogene are thought to account for many cases of steroid 21-hydroxylase deficiency. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
CYP21A2 |
| Location |
6p21.33 |
| Chromosome |
Chromosome6_ssto_hap7 |
| Coordinates |
This gene maps to 3306068-3342155 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-CYP21A2-03383-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CYP21A2-03383-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CYP21A2-03383-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CYP21A2-03383-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CYP21A2-03383-AQ |
467nm |
418nm |
|
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