Gene-specific Copy Number Variation Probe-TCL1B
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Catalog: |
CNVFP-TCL1B-20669 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TCL1B). 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: |
TCL1B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TCL1B genes. This product achieves the purpose of detection by hybridizing with the TCL1B 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 |
T-cell Leukemia/lymphoma 1B |
Gene Summary [Provided by RefSeq] |
The T-cell Leukemia/lymphoma 1B (TCL1B) gene is located on chr14:96152753 -96158980 at 14q32.13. |
Gene Symbol |
TCL1B |
Location |
14q32.13 |
Chromosome |
Chromosome14 |
Coordinates |
This gene maps to 96152753-96158980 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-TCL1B-20669-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-TCL1B-20669-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-TCL1B-20669-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-TCL1B-20669-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-TCL1B-20669-AQ |
467nm |
418nm |
|
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