Gene-specific Copy Number Variation Probe-MED26
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Catalog: |
CNVFP-MED26-11277 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MED26). 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: |
MED26 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MED26 genes. This product achieves the purpose of detection by hybridizing with the MED26 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 |
Mediator Complex Subunit 26 |
Gene Summary [Provided by RefSeq] |
The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. [provided by RefSeq, Jul 2008] |
Gene Symbol |
MED26 |
Location |
19p13.11 |
Chromosome |
Chromosome19 |
Coordinates |
This gene maps to 16685717-16739015 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-MED26-11277-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-MED26-11277-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-MED26-11277-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-MED26-11277-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-MED26-11277-AQ |
467nm |
418nm |
|
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