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IMCS

IMCS

Integrated Micro-Chromatography Systems, Inc (IMCS) is a biotechnology company focused on delivering tools and services to...

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Dive Deeper with Tymora

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In collaboration with

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Tymora's Superior Proteomics Services

Discover the full capabilities of your samples with Tymora Analytical's Proteomics Services. Using their proprietary EVtrap technology, Tymora provides a comprehensive analysis of proteins and their post-translational modifications (PTMs) from various biological samples. Identify critical biomarkers and gain a deeper understanding of intricate biological processes.

Whether you're working with plasma, urine, saliva, or tissue samples, Tymora's Proteomics Services provide a reliable platform for your research requirements. Here's what Tymora offers:

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Plasma

Probe the comprehensive protein and PTM profile of plasma-derived EVs.

Identify >1,000 unique proteins from just 10 µL plasma, or 600-1,000 unique phosphoproteins from just 0.5 mL plasma.

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Urine

Harness the power of truly non-invasive urine samples to uncover unique biomarkers.

10 mL of urine can detect 3,200 phosphopeptides and 1,200 phosphoproteins.

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Saliva

Explore the potential of saliva as a rich source of disease-specific EVs.

Identify >1,000 unique proteins from just 20 µL saliva, or 500-1,000 unique phosphoproteins from just 1 mL saliva.

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Tissue

Unearth the complex interplay of proteins and their modifications within specific tissues.

Analyze low-abundant proteins, phosphoproteins, glycoproteins, and others from frozen tissue samples.

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Cell Lysate

Get an in-depth view of the proteomic landscape of your cell cultures.

Analyze low-abundant proteins, phosphoproteins, glycoproteins, and others from frozen cells or cell lysate samples.

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Other Samples

Tymora accommodates a wide range of sample types, catering to your diverse research needs.

Custom services are available for most sample types (e.g., plant, fungi, bacteria, IP, in-gel digests, etc.).

EVtrap

Test EVtrap NOW!

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Mention IMev2023 for a special discounted rate!

Discover Powerful, Non-Invasive Biomarkers

Exosomes are extracellular vesicles generated by all cells and they carry nucleic acids, proteins, lipids, and metabolites. They are mediators of near and long-distance intercellular communication in health and disease and affect various aspects of cell biology. (Kalluri and LeBleu. Science 2020. doi: 10.1126/science.aau6977)
Exosomes are extracellular vesicles generated by all cells and they carry nucleic acids, proteins, lipids, and metabolites. They are mediators of near and long-distance intercellular communication in health and disease and affect various aspects of cell biology. (Kalluri and LeBleu. Science 2020. doi: 10.1126/science.aau6977)

Unlock new frontiers in non-invasive biomarker discovery with Tymora Analytical. Extracellular vesicles (EVs), including exosomes, offer a unique window into the health status of their originating cells by their distinct protein profiles. When isolated from urine, they present a wealth of clinically relevant data. Tymora Analytical stands at the forefront of this pioneering approach, using their proprietary EVtrap technology and Proteomics/PTMs analysis. By extracting and profiling proteins and their post-translational modifications (PTMs) from EVs in urine, they provide researchers with comprehensive insights into disease processes, helping to advance personalized medicine.

JUMPSTART YOUR PROJECT

Get your results in two to three weeks! Here's how it works:

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Analyze My Samples

Comparison of Extracellular Vesicle (EV) Purification and Isolation Methods

wdt_ID Principle/Method Benefits Disadvantages Processing Time Reported Purity Reported Yield References
1 EVtrap High yield, purity and
reproducibility.
Compatible with
proteomics analysis,
automatable, easy
to use with standard equipment.
Higher cost,
elution buffer
needs to be dried
or neutralized.
< 1 hour High (>99%) High (>95%)

1-3

2 Ultracentrifugation Current benchmark Time consuming,
low yield,
cumbersome process,
may damage exosomes
> 4 hours Medium Medium

4

3 Density gradient centrifugation High purity, avoiding
exosomal damage
Labor-intensive,
preliminary preparation
and cumbersome
operation
>16 h High Low

5

4 Ultrafiltration Easy, without special
equipment and
reagents
Clogging on filtering
membrane, loss of
exosomes of small
particle diameter
Generally <4 h High Medium

6

5 Size exclusion chromatography Simple, economical,
maintain the
biological function
and structure
Special columns and
packing are required,
lipoprotein
contamination
0.3 h for qEV High High 7
6 Immunoaffinity High specificity for
exosome subtypes
isolation
Expensive, depending
on specificity of the
antibody
4–20 h High Medium 8
7 Polymer co-precipitation Simple operation,
suitable for large-volume
samples
Potential contaminants
(co-purifying protein
aggregates or residuary
polymers)
≈0.3–12 h Low High

8

(Table modified from Chen J, Li P, Zhang T, Xu Z, Huang X, Wang R, Du L. (2022). Review on strategies and technologies for exosome isolation and purification. Front. Bioeng. Biotechnol. doi: 10.3389/fbioe.2021.811971.)

REFERENCES
REFERENCES
  1. Iliuk AB. (2022). Purification and Phosphoproteomic Analysis of Plasma-Derived Extracellular Vesicles. Methods Mol Biol. doi: 10.1007/978-1-0716-2341-1_11.
  2. Iliuk A, Wu X, Li L, Sun J, Hadisurya M, Boris RS, Tao WA. (2020). Plasma-Derived Extracellular Vesicle Phosphoproteomics through Chemical Affinity Purification. J Proteome Res. doi: 10.1021/acs.jproteome.0c00151.
  3. Wu X, Li L, Iliuk A, Tao WA. (2018). Highly Efficient Phosphoproteome Capture and Analysis from Urinary Extracellular Vesicles. J Proteome Res. doi: 10.1021/acs.jproteome.8b00459.
  4. Lin S, Yu Z, Chen D, Wang Z, Miao J, Li Q, et al. (2020). Progress in Microfluidics-Based Exosome Separation and Detection Technologies for Diagnostic Applications. Small. doi:10.1002/smll.201903916
  5. Kamerkar S, Lebleu VS, Sugimoto H, Yang S, Ruivo CF, Melo SA, et al. (2017). Exosomes Facilitate Therapeutic Targeting of Oncogenic KRAS in Pancreatic Cancer. Nature. doi:10.1038/nature22341
  6. Ding L, Yang X, Gao Z, Effah CY, Zhang X,Wu Y, et al. (2021). A Holistic Review of the State-of-the-Art Microfluidics for Exosome Separation: An Overview of the Current Status, Existing Obstacles, and Future Outlook. Small. doi:10.1002/smll.202007174
  7. Mohammadi M, Zargartalebi H, Salahandish R, Aburashed R, Wey Yong K, and Sanati-Nezhad, A. (2021). Emerging Technologies and Commercial Products in Exosome-Based Cancer Diagnosis and Prognosis. Biosens. Bioelectron. doi:10.1016/j.bios.2021.113176
  8. Coumans FAW, Brisson AR, Buzas EI, Dignat-George F, Drees EEE, El-Andaloussi S., et al. (2017). Methodological Guidelines to Study Extracellular Vesicles. Circ. Res. doi:10.1161/CIRCRESAHA.117.309417
EVtrap

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Mention IMev2023 for a special discounted rate!

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ABOUT

ABOUT IMCS

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RESEARCH AT IMCS

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