Gene-specific Copy Number Variation Probe-TSN
Add to Cart
| Catalog: |
CNVFP-TSN-22285 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TSN). 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: |
TSN Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TSN genes. This product achieves the purpose of detection by hybridizing with the TSN 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 |
Translin |
| Gene Summary [Provided by RefSeq] |
This gene encodes a DNA-binding protein which specifically recognizes conserved target sequences at the breakpoint junction of chromosomal translocations. Translin polypeptides form a multimeric structure that is responsible for its DNA-binding activity. Recombination-associated motifs and translin-binding sites are present at recombination hotspots and may serve as indicators of breakpoints in genes which are fused by translocations. These binding activities may play a crucial role in chromosomal translocation in lymphoid neoplasms. This protein encoded by this gene, when complexed with translin-associated protein X, also forms a Mg ion-dependent endoribonuclease that promotes RNA-induced silencing complex (RISC) activation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2012] |
| Gene Symbol |
TSN |
| Location |
2q14.3 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 122513120-122525428 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-TSN-22285-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TSN-22285-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TSN-22285-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TSN-22285-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TSN-22285-AQ |
467nm |
418nm |
|
Other Products
