Gene-specific Copy Number Variation Probe-BCL10
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Catalog: |
CNVFP-BCL10-01412 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BCL10). 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: |
BCL10 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BCL10 genes. This product achieves the purpose of detection by hybridizing with the BCL10 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 10 |
Gene Summary [Provided by RefSeq] |
This gene was identified by its translocation in a case of mucosa-associated lymphoid tissue (MALT) lymphoma. The protein encoded by this gene contains a caspase recruitment domain (CARD), and has been shown to induce apoptosis and to activate NF-kappaB. This protein is reported to interact with other CARD domain containing proteins including CARD9, 10, 11 and 14, which are thought to function as upstream regulators in NF-kappaB signaling. This protein is found to form a complex with MALT1, a protein encoded by another gene known to be translocated in MALT lymphoma. MALT1 and this protein are thought to synergize in the activation of NF-kappaB, and the deregulation of either of them may contribute to the same pathogenetic process that leads to the malignancy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016] |
Gene Symbol |
BCL10 |
Location |
1p22.3 |
Chromosome |
Chromosome1 |
Coordinates |
This gene maps to 85731459-85742587 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-BCL10-01412-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-BCL10-01412-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-BCL10-01412-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-BCL10-01412-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-BCL10-01412-AQ |
467nm |
418nm |
|
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