Gene-specific Copy Number Variation Probe-TAB2
Add to Cart
| Catalog: |
CNVFP-TAB2-20202 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TAB2). 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: |
TAB2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TAB2 genes. This product achieves the purpose of detection by hybridizing with the TAB2 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 |
TGF-beta Activated Kinase 1/MAP3K7 Binding Protein 2 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is an activator of MAP3K7/TAK1, which is required for for the IL-1 induced activation of nuclear factor kappaB and MAPK8/JNK. This protein forms a kinase complex with TRAF6, MAP3K7 and TAB1, and it thus serves as an adaptor that links MAP3K7 and TRAF6. This protein, along with TAB1 and MAP3K7, also participates in the signal transduction induced by TNFSF11/RANKl through the activation of the receptor activator of NF-kappaB (TNFRSF11A/RANK), which may regulate the development and function of osteoclasts. Studies of the related mouse protein indicate that it functions to protect against liver damage caused by chemical stressors. Mutations in this gene cause congenital heart defects, multiple types, 2 (CHTD2). Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014] |
| Gene Symbol |
TAB2 |
| Location |
6q25.1 |
| Chromosome |
Chromosome6 |
| Coordinates |
This gene maps to 149639435-149732747 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-TAB2-20202-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TAB2-20202-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TAB2-20202-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TAB2-20202-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TAB2-20202-AQ |
467nm |
418nm |
|
Other Products
