Gene-specific Copy Number Variation Probe-RUNX1T1
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| Catalog: |
CNVFP-RUNX1T1-17690 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RUNX1T1). 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: |
RUNX1T1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RUNX1T1 genes. This product achieves the purpose of detection by hybridizing with the RUNX1T1 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 |
RUNX1 Translocation Partner 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the myeloid translocation gene family which interact with DNA-bound transcription factors and recruit a range of corepressors to facilitate transcriptional repression. The t(8;21)(q22;q22) translocation is one of the most frequent karyotypic abnormalities in acute myeloid leukemia. The translocation produces a chimeric gene made up of the 5'-region of the runt-related transcription factor 1 gene fused to the 3'-region of this gene. The chimeric protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010] |
| Gene Symbol |
RUNX1T1 |
| Location |
8q21.3 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 92967194-93115454 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-RUNX1T1-17690-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RUNX1T1-17690-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RUNX1T1-17690-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RUNX1T1-17690-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RUNX1T1-17690-AQ |
467nm |
418nm |
|
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