Gene-specific Copy Number Variation Probe-KRT8
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| Catalog: |
CNVFP-KRT8-08190 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KRT8). 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: |
KRT8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KRT8 genes. This product achieves the purpose of detection by hybridizing with the KRT8 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 |
Keratin 8 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012] |
| Gene Symbol |
KRT8 |
| Location |
12q13.13 |
| Chromosome |
Chromosome12 |
| Coordinates |
This gene maps to 53290970-53298868 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-KRT8-08190-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-KRT8-08190-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-KRT8-08190-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-KRT8-08190-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-KRT8-08190-AQ |
467nm |
418nm |
|
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