Gene-specific Copy Number Variation Probe-BCL7B
Add to Cart
| Catalog: |
CNVFP-BCL7B-01431 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BCL7B). 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: |
BCL7B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BCL7B genes. This product achieves the purpose of detection by hybridizing with the BCL7B 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 |
BCL Tumor Suppressor 7B |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the BCL7 family including BCL7A, BCL7B and BCL7C proteins. This member is BCL7B, which contains a region that is highly similar to the N-terminal segment of BCL7A or BCL7C proteins. The BCL7A protein is encoded by the gene known to be directly involved in a three-way gene translocation in a Burkitt lymphoma cell line. This gene is located at a chromosomal region commonly deleted in Williams syndrome. This gene is highly conserved from C. elegans to human. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2010] |
| Gene Symbol |
BCL7B |
| Location |
7q11.23 |
| Chromosome |
Chromosome7 |
| Coordinates |
This gene maps to 72950682-72972065 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-BCL7B-01431-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-BCL7B-01431-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-BCL7B-01431-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-BCL7B-01431-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-BCL7B-01431-AQ |
467nm |
418nm |
|
Other Products
