Gene-specific Copy Number Variation Probe-SEPT5-GP1BB
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| Catalog: |
CNVFP-SEPT5-GP1BB-18233 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SEPT5-GP1BB). 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: |
SEPT5-GP1BB Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SEPT5-GP1BB genes. This product achieves the purpose of detection by hybridizing with the SEPT5-GP1BB 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 |
SEPT5-GP1BB Readthrough |
| Gene Summary [Provided by RefSeq] |
This locus represents naturally occurring read-through transcription between the neighboring SEPT5 (septin 5) and GP1BB (glycoprotein Ib (platelet), beta polypeptide) genes on chromosome 22. This read-through transcription arises from inefficient use of an imperfect polyA signal in the upstream SEPT5 gene, whereby transcription continues into the GP1BB gene. Alternative splicing results in multiple read-through variants. The read-through transcripts are candidates for nonsense-mediated mRNA decay (NMD), and are therefore unlikely to produce protein products. [provided by RefSeq, Dec 2010] |
| Gene Symbol |
SEPT5-GP1BB |
| Location |
22q11.21 |
| Chromosome |
Chromosome22 |
| Coordinates |
This gene maps to 19704742-19712297 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-SEPT5-GP1BB-18233-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SEPT5-GP1BB-18233-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SEPT5-GP1BB-18233-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SEPT5-GP1BB-18233-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SEPT5-GP1BB-18233-AQ |
467nm |
418nm |
|
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