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Phospho-Specific Antibodies

 

Detect site-specific protein phosphorylation with Biorbyt antibodies for Ser, Thr and Tyr phosphorylation events across major cell-signaling pathways.

Browse by signaling pathway or exact phospho site, then use the experimental guidance below to plan stimulation, preserve phospho-state and interpret phospho-specific signals alongside total protein.

Phospho-specific antibody binding a phosphorylated protein site in cell signaling research

Browse Phospho Antibodies by Signaling Pathway

Start with the signaling pathway you are studying and open the corresponding Biorbyt pathway guide for biological context, pathway components and research tools.

MAPK phosphorylation cascade showing MEK, ERK, JNK and p38 signaling

MAPK Signaling

Study phosphorylation across the RAF-MEK-ERK cascade and stress-activated JNK and p38 MAPK branches using site-specific phospho antibodies.

AKT mTOR phosphorylation signaling with mTORC1 mTORC2 S6 kinase and ribosomal S6 targets

mTOR Signaling

Follow phosphorylation across the AKT-mTOR axis, including mTORC1/2 signaling and downstream control of translation, growth and metabolism.

More Phosphorylation-Relevant Pathways & Research Areas

Explore additional Biorbyt pathway and research-area guides where phosphorylation is an important regulatory mechanism or experimental readout.

Planning a Phosphorylation Experiment

Phosphorylation is dynamic, site-specific and highly dependent on stimulation conditions. A useful phospho experiment starts with the biological event you want to measure, then controls sample handling and interpretation around that event.

1

Choose the biological readout, not just the protein

Different sites on the same target can report different regulatory events. For example, AKT Ser473 and Thr308 should not automatically be treated as interchangeable readouts. Select the phospho site that matches your pathway question.

2

Plan stimulus, dose and time point

Growth factors, cytokines, stressors and drugs can produce rapid and transient phospho responses. If the kinetics are uncertain, use a time-course or dose-response design rather than relying on a single endpoint.

3

Preserve the phospho-state during sample handling

For lysate-based assays, harvest rapidly, work cold where appropriate and include compatible phosphatase inhibitors. Protease inhibitors protect protein integrity but do not replace phosphatase inhibitors. For phospho-flow, fixation timing is part of the measurement because signaling can continue after stimulation.

4

Build controls around pathway activation

Include stimulated and unstimulated samples, and pathway inhibitors or other mechanistic controls where appropriate. Pair phospho-specific detection with the corresponding total target when you need to separate phosphorylation changes from changes in protein abundance.

Stimulated vs. unstimulated
Phosphatase inhibition
Phospho + total target
Pathway-specific control

Phospho-Specific Antibody vs. Total Antibody

Phospho-Specific Antibody

Designed to preferentially recognise a target when a defined residue is phosphorylated. Use it to ask whether a specific phosphorylation event changes after stimulation, inhibition or treatment.

Total-Target Antibody

Measures overall target abundance without selecting for one defined phospho-state. Use it to determine whether an apparent phospho change may also reflect a change in total protein abundance.

Interpretation tip: for quantitative assays such as Western blotting, phospho and total signals can be evaluated together using an appropriate normalization strategy. For imaging or flow-based assays, interpret phospho-state in the context of the assay design and controls rather than assuming a simple phospho/total ratio is always appropriate.

Need help selecting a phospho-specific antibody?

Our scientific support team can help compare phosphorylation sites, pathway context, species reactivity, applications and validation data.

Contact Tech Support

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