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Overview
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Product nameAnti-PKC gamma antibody [EPR2750]
See all PKC gamma primary antibodies -
DescriptionRabbit monoclonal [EPR2750] to PKC gamma
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Host speciesRabbit
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Tested applicationsSuitable for: WB, ICCmore details
Unsuitable for: Flow Cyt,IHC-P or IP -
Species reactivityReacts with: Mouse, Rat, Human
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Immunogen
Synthetic peptide within Human PKC gamma (C terminal). The exact sequence is proprietary.
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Positive control
- Human fetal brain and Human fetal cerebellum cell lysates
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General notes
A trial size is available to purchase for this antibody.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMab® patents
This product is a recombinant rabbit monoclonal antibody.
Properties
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FormLiquid
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Storage instructionsShipped at 4°C. Store at -20°C. Stable for 12 months at -20°C.
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Storage bufferpH: 7.20
Preservative: 0.05% Sodium azide
Constituents: 0.1% BSA, 40% Glycerol, 9.85% Tris glycine, 50% Tissue culture supernatant -
PurityTissue culture supernatant
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ClonalityMonoclonal
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Clone numberEPR2750
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IsotypeIgG
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Research areas
Applications
Our Abpromise guarantee covers the use of ab108961 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
| Application | Abreviews | Notes |
|---|---|---|
| WB | 1/1000 - 1/10000. Detects a band of approximately 80 kDa (predicted molecular weight: 78 kDa). | |
| ICC | 1/50. |
Target
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FunctionThis is a calcium-activated, phospholipid-dependent, serine- and threonine-specific enzyme.
PKC is activated by diacylglycerol which in turn phosphorylates a range of cellular proteins. PKC also serves as the receptor for phorbol esters, a class of tumor promoters. -
Tissue specificityExpressed in Purkinje cells of the cerebellar cortex.
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Involvement in diseaseDefects in PRKCG are the cause of spinocerebellar ataxia type 14 (SCA14) [MIM:605361]. Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA14 is an autosomal dominant cerebellar ataxia (ADCA).
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Sequence similaritiesBelongs to the protein kinase superfamily. AGC Ser/Thr protein kinase family. PKC subfamily.
Contains 1 AGC-kinase C-terminal domain.
Contains 1 C2 domain.
Contains 2 phorbol-ester/DAG-type zinc fingers.
Contains 1 protein kinase domain. - Information by UniProt
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Database links
- Entrez Gene: 5582 Human
- Entrez Gene: 18752 Mouse
- Entrez Gene: 24681 Rat
- Omim: 176980 Human
- SwissProt: P05129 Human
- SwissProt: P63318 Mouse
- SwissProt: P63319 Rat
- Unigene: 631564 Human
see all -
Alternative names
- KPCG_HUMAN antibody
- MGC57564 antibody
- OTTHUMP00000067291 antibody
see all
Images
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![Western blot - Anti-PKC gamma antibody [EPR2750] (ab108961)](https://www.abcam.com/ps/products/108/ab108961/Images/PKC-gamma-Primary-antibodies-ab108961-2.JPG)
Western blot - Anti-PKC gamma antibody [EPR2750] (ab108961)All lanes : Anti-PKC gamma antibody [EPR2750] (ab108961) at 1/1000 dilution
Lane 1 : Human fetal brain cell lysate
Lane 2 : Human fetal cerebellum cell lysate
Lysates/proteins at 10 µg per lane.
Predicted band size: 78 kDa
References
ab108961 has not yet been referenced specifically in any publications.
Customer reviews and Q&As
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"