v-innovate Technologies provides cytokinin (CTK or CK) analysis in plants using liquid chromatography with tandem mass spectrometry (LC-MS/MS), which can ensure ultrahigh recovery rates, sufficient robustness, enhanced sensitivity, and high resolution for accurate identification and quantification of cytokinins. Our end-to-end solutions can help researchers better understand cytokinins, including their roles in plant growth and agriculture.
Cytokinins are N6-substituted adenine derivatives that have been implicated in numerous aspects of plant growth and development, including cell seed germination, de-etiolation, apical dominance, chloroplast differentiation, sink/source relationships, nutrient uptake, flower and fruit development, leaf senescence, and response to biotic and abiotic factors. The most common cytokinins have isoprenoid side chains, but there are also adenine derivatives with aromatic substituents, as well as synthetic cytokinins derived from diphenylurea (DPU). The structure and conformation of side chains are vital to the activity of cytokinins. For example, trans-zeatin is one of the most abundant cytokinins present in higher plants that displays a high activity in bioassays, but the cis-isomer displays a significantly lower activity. Determination of the distribution and content of the various cytokinins in a given plant tissue provides valuable insights into the molecular mechanisms underlying the action of cytokinins.
Figure 1. Structures of cytokinins (Kieber et al., 2014).
v-innovate Technologies has optimized sample preprocessing methods to ensure efficiency and ultrahigh recovery rates consistently exceeding 85%. Mass spectrometry combined with our optimized sample preprocessing methods and other instrumentation offers precise detection down to ultra-trace levels.
Figure 2. Cytokinins analysis service workflow.
Quantification methods: external reference method or isotope-labeled internal standard method
Mode: MRM, capable of simultaneously detecting more than 1000 MRM ion pairs
Precision: ≤10-9 g
Positive/Negative polarity switching time: ≤20 ms, allowing for the acquisition of Q1/Q3 MRM transition mass spectra in both ionization modes from a single LC-MS/MS run.
Detectable CTKs | CAS | Quantification Methods |
---|---|---|
N6-(Δ2-isopentenyl)-adenine (IP) | 2365-40-4 | External reference method / isotope-labeled internal standard method |
IPA (isopentenyladenosine) | 7724-76-7 | External reference method / isotope-labeled internal standard method |
Benzylaminopurine (6-BA) | 1214-39-7 | External reference method / isotope-labeled internal standard method |
Kinetin (KT) | 525-79-1 | External reference method / isotope-labeled internal standard method |
trans-zeatin ribotide (tZR) | 6025-53-2 | External reference method / isotope-labeled internal standard method |
(trans-zeatin) tZ | 1637-39-4 | External reference method / isotope-labeled internal standard method |
1. Fresh plant tissues: >1 g or > 0.2 mL. Provide young plant tissues for best results. Samples should be frozen in liquid nitrogen immediately after collection, and then transferred to -80°C for storage.
2. Plant seeds.
At least 3 biological replicates.
v-innovate Technologies provides high-throughput detection and quantitation of cytokinins based on state-of-the-art LC-MS platforms in a fast and sensitive manner. Our service offers maximized recovery rates and accurate profiling of cytokinins, as well as tailored statistical analysis and bioinformatics analysis to achieve reliable cytokinins analysis results.
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