Gene-specific Copy Number Variation Probe-PRKCG
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| Catalog: |
CNVFP-PRKCG-16284 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PRKCG). 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: |
PRKCG Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PRKCG genes. This product achieves the purpose of detection by hybridizing with the PRKCG 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 Gamma |
| 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 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 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 distinct roles in cells. The protein encoded by this gene is one of the PKC family members. This protein kinase is expressed solely in the brain and spinal cord and its localization is restricted to neurons. It has been demonstrated that several neuronal functions, including long term potentiation (LTP) and long term depression (LTD), specifically require this kinase. Knockout studies in mice also suggest that this kinase may be involved in neuropathic pain development. Defects in this protein have been associated with neurodegenerative disorder spinocerebellar ataxia-14 (SCA14). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015] |
| Gene Symbol |
PRKCG |
| Location |
19q13.42 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 54385466-54410901 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-PRKCG-16284-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PRKCG-16284-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PRKCG-16284-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PRKCG-16284-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PRKCG-16284-AQ |
467nm |
418nm |
|
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