Gene-specific Copy Number Variation Probe-PRKCH
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Catalog: |
CNVFP-PRKCH-16285 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PRKCH). 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: |
PRKCH Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PRKCH genes. This product achieves the purpose of detection by hybridizing with the PRKCH 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 |
Protein Kinase C Eta |
Gene Summary [Provided by RefSeq] |
Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and the second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play a distinct role in cells. The protein encoded by this gene is one of the PKC family members. It is a calcium-independent and phospholipids-dependent protein kinase. It is predominantly expressed in epithelial tissues and has been shown to reside specifically in the cell nucleus. This protein kinase can regulate keratinocyte differentiation by activating the MAP kinase MAPK13 (p38delta)-activated protein kinase cascade that targets CCAAT/enhancer-binding protein alpha (CEBPA). It is also found to mediate the transcription activation of the transglutaminase 1 (TGM1) gene. Mutations in this gene are associated with susceptibility to cerebral infarction. [provided by RefSeq, Sep 2015] |
Gene Symbol |
PRKCH |
Location |
14q23.1 |
Chromosome |
Chromosome14 |
Coordinates |
This gene maps to 61788514-62017698 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-PRKCH-16285-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-PRKCH-16285-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-PRKCH-16285-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-PRKCH-16285-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-PRKCH-16285-AQ |
467nm |
418nm |
|
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