Gene-specific Copy Number Variation Probe-APOBEC3B
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| Catalog: |
CNVFP-APOBEC3B-00886 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (APOBEC3B). 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: |
APOBEC3B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to APOBEC3B genes. This product achieves the purpose of detection by hybridizing with the APOBEC3B 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 |
Apolipoprotein B MRNA Editing Enzyme Catalytic Subunit 3B |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. It is thought that the proteins may be RNA editing enzymes and have roles in growth or cell cycle control. A hybrid gene results from the deletion of approximately 29.5 kb of sequence between this gene, APOBEC3B, and the adjacent gene APOBEC3A. The breakpoints of the deletion are within the two genes, so the deletion allele is predicted to have the promoter and coding region of APOBEC3A, but the 3' UTR of APOBEC3B. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2012] |
| Gene Symbol |
APOBEC3B |
| Location |
22q13.1 |
| Chromosome |
Chromosome22 |
| Coordinates |
This gene maps to 39378404-39388783 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-APOBEC3B-00886-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-APOBEC3B-00886-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-APOBEC3B-00886-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-APOBEC3B-00886-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-APOBEC3B-00886-AQ |
467nm |
418nm |
|
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