Polyclonal Antibodies
Anti-PKC zeta Polyclonal Antibody for WB, IF/ICC, ELISA - Q05513
Item Number : CM0029470
Price varies based on specs and customizations
- Application
- WB, IF/ICC, ELISA
- Cross Reactivity
- Human, Mouse, Rat
- Protein Weight
- 68kDa
Shipping:
Contact us to get shipping details Enjoy On-time Dispatch Guarantee.
Why Choose Us
Easy ordering process, quality products, and dedicated support for your business success.
Core Product Specifications and Parameters
| Parameter | Value |
|---|---|
| Product Name | PKC zeta Rabbit pAb |
| Remarks/Alias | PKC2; PKC-ZETA; PKC zeta |
| Species | Human |
| Gene ID (Human) | 5590 |
| Gene ID | 5590 |
| Immunogen | Recombinant fusion protein containing a sequence corresponding to amino acids 476-547 of human PKC zeta (NP_002735.3). |
| Source | Rabbit |
| Category | Polyclonal Antibodies |
| Application | WB, IF/ICC, ELISA |
| Cross Reactivity | Human, Mouse, Rat |
| SWISS | Q05513 |
| Protein Weight | 68kDa |
| Shipping | Ice bag |
Biological Background: PKC zeta Function and Localization
- PKC zeta (nPKC-zeta) is an atypical protein kinase C, lacking calcium and diacylglycerol sensitivity, and functions as a serine/threonine-protein kinase in NF-kappa-B activation, mitogenic signaling, cell proliferation, cell polarity, inflammatory response, and maintenance of long-term potentiation (LTP).
- Downstream of PI3K, PKC zeta activates the MEK1-ERK2 cascade independently of RAF1 in macrophages and following mitogenic stimuli. It also contributes to insulin-dependent AKT3 activation and GLUT4 translocation in adipocytes, acting partly as an adapter.
- PKC zeta mediates NF-kappa-B activation via interactions with SQSTM1/p62, RIPK1, and TRAF6, leading to IKBKB phosphorylation and NF-kappa-B inhibitor degradation. It further phosphorylates RELA at Ser-311 to counteract SETD6-mediated repression.
- In cell polarity, PKC zeta forms a cytoplasmic complex with PARD6A and is recruited by CDC42 to establish polarity with microtubule motors. It stimulates neuronal differentiation with FEZ1 and is required for late-phase LTP in hippocampal CA1 synapses, crucial for long-term memory.
- PKC zeta phosphorylates VAMP2 in vitro and activates LRRK1, which then phosphorylates RAB proteins involved in intracellular trafficking. Related references: PMID:17313651 PMID:36040231
- PKC zeta localizes to the cytoplasm, endosomes, cell junctions, and membrane. It is predominantly expressed in the brain, with lower levels in lung, kidney, and testis. It contains a zinc-finger domain and ATP-binding site, and is subject to alternative splicing and phosphorylation.
Experimental Guidance and Technical Tips
- The immunogen corresponds to the C-terminal region (amino acids 476–547), which may provide good epitope accessibility for native and denatured protein detection.
- For Western blotting, the predicted molecular weight is ~68 kDa; always include positive and negative controls to confirm specificity.
- In immunofluorescence/ICC, optimize fixation and permeabilization conditions, as PKC zeta can localize to multiple compartments (cytoplasm, membrane, endosomes, junctions).
- ELISA can be used for quantitative detection of PKC zeta in cell lysates or purified protein; validate with known standards.
- Cross-reactivity with mouse and rat is expected; confirm reactivity in your specific sample system before large-scale studies.
CamelBio: Your One-Stop Sourcing Bridge
CamelBio serves diagnostic manufacturers and research labs with convenient access to IVD raw materials, technical services, and consulting from concept to clinic. This anti-PKC zeta antibody supports investigations into cell signaling, cancer biology, and inflammatory pathways. Beyond single reagents, CamelBio offers validated antibody pairs, optimized monoclonal and polyclonal antibodies, bulk ancillary reagents, and rare target raw-material sourcing to streamline your development workflow.
REQUEST A QUOTE
Our professional team will reply to you within one business day. Please feel free to contact us!
Related Articles
Matrix Interference in ELISA Development: Designing Accuracy Into Complex-Sample Assays
Learn how to diagnose and control ELISA matrix interference through sample cleanup, buffer design, calibration, and smarter reagent selection.
From Matrix Noise to Measurable Signal: A Practical Extraction Strategy for ELISA Testing
Learn how pentane extraction, alkaline back-extraction, and neutral buffering remove matrix effects before sensitive ELISA analysis.
When the Dye Sees Everything: A Systematic Strategy for Cleaner, More Reliable qPCR
Learn how primer design, Mg2+ control, thermal optimization, and melt curves reduce background signal in dye-based qPCR assays.
qPCR Primer Design: The Small Decisions That Determine Assay Reliability
A practical guide to qPCR primer design, from amplicon length and 3' stability to validation for efficient, reproducible diagnostics.
Why Direct Hapten Coupling Changes the Economics of Small-Molecule Biosensors
Compare direct hapten coupling with protein conjugates to improve ligand density, signal quality, antibody efficiency, and chip reusability.
The Thermal Block Is the Hidden Variable in Real-Time PCR Performance
How ramp rate, gradient control, block geometry, and thermal uniformity shape qPCR speed, optimization, reproducibility, and sample volume.
ROX in qPCR: The Quiet Reference That Makes Diagnostic Signals Trustworthy
Learn how ROX normalizes qPCR fluorescence, stabilizes Ct calls, and shapes the trade-off between instrument compatibility and multiplexing.
When the Seal Changes the Result: Controlling CT Variance in Real-Time PCR
Learn how evaporation, optical interference, and edge effects raise qPCR CT values, and how better sealing protects diagnostic accuracy.
Why Thermal Ramp Rates and Gradient Control Decide the Quality of a qPCR Assay
Learn how qPCR ramp rates and thermal gradients reduce run time, improve uniformity, and rapidly identify the annealing temperature for reliable diagnostics.
Choosing the Thermal Architecture That Makes a Molecular Assay Transferable
Compare Peltier blocks and air-heated carousels across speed, uniformity, sample flexibility, optimization, and throughput for qPCR development.
Two Positive Controls, One Clear Answer: Isolating RT and PCR Failure in qRT-PCR Diagnostics
Learn how dual positive controls isolate reverse transcription and PCR failures, improve qRT-PCR reliability, and support compliant diagnostic workflows.
From Molecular Recognition to Reliable Results: Engineering Biosensors for Rapid Safety Testing
How antibodies and enzymes turn invisible molecular events into reliable biosensor signals, and how material quality determines test performance.