Gene-specific Copy Number Variation Probe-BCL11A
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| Catalog: |
CNVFP-BCL11A-01411 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BCL11A). 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: |
BCL11A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BCL11A genes. This product achieves the purpose of detection by hybridizing with the BCL11A 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 |
B-cell CLL/lymphoma 11A |
| Gene Summary [Provided by RefSeq] |
This gene encodes a C2H2 type zinc-finger protein by its similarity to the mouse Bcl11a/Evi9 protein. The corresponding mouse gene is a common site of retroviral integration in myeloid leukemia, and may function as a leukemia disease gene, in part, through its interaction with BCL6. During hematopoietic cell differentiation, this gene is down-regulated. It is possibly involved in lymphoma pathogenesis since translocations associated with B-cell malignancies also deregulates its expression. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
BCL11A |
| Location |
2p16.1 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 60678301-60780633 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-BCL11A-01411-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-BCL11A-01411-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-BCL11A-01411-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-BCL11A-01411-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-BCL11A-01411-AQ |
467nm |
418nm |
|
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