Gene-specific Copy Number Variation Probe-STAT5B
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| Catalog: |
CNVFP-STAT5B-20156 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (STAT5B). 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: |
STAT5B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to STAT5B genes. This product achieves the purpose of detection by hybridizing with the STAT5B 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 |
Signal Transducer And Activator Of Transcription 5B |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the STAT family of transcription factors. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein mediates the signal transduction triggered by various cell ligands, such as IL2, IL4, CSF1, and different growth hormones. It has been shown to be involved in diverse biological processes, such as TCR signaling, apoptosis, adult mammary gland development, and sexual dimorphism of liver gene expression. This gene was found to fuse to retinoic acid receptor-alpha (RARA) gene in a small subset of acute promyelocytic leukemias (APLL). The dysregulation of the signaling pathways mediated by this protein may be the cause of the APLL. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
STAT5B |
| Location |
17q21.2 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 40351194-40428424 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-STAT5B-20156-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-STAT5B-20156-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-STAT5B-20156-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-STAT5B-20156-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-STAT5B-20156-AQ |
467nm |
418nm |
|
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