Gene-specific Copy Number Variation Probe-BORCS8-MEF2B
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| Catalog: |
CNVFP-BORCS8-MEF2B-01560 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BORCS8-MEF2B). 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: |
BORCS8-MEF2B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BORCS8-MEF2B genes. This product achieves the purpose of detection by hybridizing with the BORCS8-MEF2B 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 |
BORCS8-MEF2B Readthrough |
| Gene Summary [Provided by RefSeq] |
This gene represents numerous read-through transcripts that span GeneID:729991 and 100271849. Many read-through transcripts are predicted to be nonsense-mediated decay (NMD) candidates, and are thought to be non-coding. Some transcripts are predicted to be capable of translation reinitiation at a downstream AUG, resulting in expression of at least one isoform of myocyte enhancer factor 2B (MEF2B) from this read-through locus. At least one additional MEF2B variant and isoform can be expressed from a downstream promoter, and is annotated on GeneID:100271849. [provided by RefSeq, Oct 2010] |
| Gene Symbol |
BORCS8-MEF2B |
| Location |
19p13.11 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 19192590-19145566 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-BORCS8-MEF2B-01560-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-BORCS8-MEF2B-01560-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-BORCS8-MEF2B-01560-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-BORCS8-MEF2B-01560-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-BORCS8-MEF2B-01560-AQ |
467nm |
418nm |
|
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