Gene-specific Copy Number Variation Probe-VIM
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| Catalog: |
CNVFP-VIM-22850 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (VIM). 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: |
VIM Gene-specific copy number variation probes are mainly used to detect the copy number variation related to VIM genes. This product achieves the purpose of detection by hybridizing with the VIM 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 |
Vimentin |
| Gene Summary [Provided by RefSeq] |
This gene encodes a type III intermediate filament protein. Intermediate filaments, along with microtubules and actin microfilaments, make up the cytoskeleton. The encoded protein is responsible for maintaining cell shape and integrity of the cytoplasm, and stabilizing cytoskeletal interactions. This protein is involved in neuritogenesis and cholesterol transport and functions as an organizer of a number of other critical proteins involved in cell attachment, migration, and signaling. Bacterial and viral pathogens have been shown to attach to this protein on the host cell surface. Mutations in this gene are associated with congenital cataracts in human patients. [provided by RefSeq, Aug 2017] |
| Gene Symbol |
VIM |
| Location |
10p13 |
| Chromosome |
Chromosome10 |
| Coordinates |
This gene maps to 17270257-17279592 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-VIM-22850-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-VIM-22850-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-VIM-22850-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-VIM-22850-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-VIM-22850-AQ |
467nm |
418nm |
|
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