Prof. Dr. rer. nat. Janina Kneipp
Profil
Forschungsthemen12
Charakterisierung natürlicher Bioaerosole
Quelle ↗Förderer: DFG Sachbeihilfe Zeitraum: 10/2008 - 07/2014 Projektleitung: Prof. Dr. rer. nat. Janina Kneipp
Combined FTIR and Raman analysis of pollen composition for studying plant adaptation to environmental changes
Quelle ↗Förderer: DAAD Zeitraum: 01/2014 - 12/2017 Projektleitung: Prof. Dr. rer. nat. Janina Kneipp
DYnamic control in hybrid plasmonic NAnopores: road to next generation multiplexed single MOlecule detection
Quelle ↗Förderer: Horizon Europe: Doctoral Network DN Zeitraum: 09/2022 - 08/2026 Projektleitung: Prof. Dr. rer. nat. Janina Kneipp
ERC: Multiphoton Processes Using Plasmonics: Towards Advanced Nanobiophotonics (MULTIBIOPHOT)
Quelle ↗Zeitraum: 01/2011 - 12/2015 Projektleitung: Prof. Dr. rer. nat. Janina Kneipp
EXC 2008: Unifying Systems in Catalysis (UniSysCat)
Quelle ↗Förderer: DFG Exzellenzstrategie Cluster Zeitraum: 01/2019 - 12/2025 Projektleitung: Prof. Dr. Arne Thomas
EXC 314/1 AG Kneipp
Quelle ↗Förderer: DFG Exzellenzstrategie Cluster Zeitraum: 01/2019 - 12/2020 Projektleitung: Prof. Dr. rer. nat. Janina Kneipp
FOR 2177/1: Inline SERS-Charakterisierung in mikrofluidischen Reaktionssystemen (TP 03)
Quelle ↗Förderer: DFG Forschungsgruppe Zeitraum: 10/2015 - 03/2020 Projektleitung: Prof. Dr. rer. nat. Janina Kneipp
Größenskalen in der molekularen Bildgebung verbinden: Eine Synchrotron-Mikroskopie-Station für räumliche, zeitliche und polarisationsaufgelöste Schwingungsspektroskopie
Quelle ↗Förderer: Bundesministerium für Forschung, Technologie und Raumfahrt Zeitraum: 07/2019 - 11/2023 Projektleitung: Prof. Dr. rer. nat. Janina Kneipp
Monitoring enzyme function at lipid membranes by SERS
Quelle ↗Förderer: Einstein Zentrum Zeitraum: 01/2021 - 12/2023 Projektleitung: Prof. Dr. rer. nat. Janina Kneipp
Silica incorporation into newly synthesized cell walls and its effects on physiological properties of plant cells
Quelle ↗Förderer: Einstein Stiftung Berlin Zeitraum: 05/2012 - 12/2015 Projektleitung: Prof. Dr. rer. nat. Janina Kneipp
Struktur und Wechselwirkung von Enzyminetzwerken und ihren Metaboliten in situ mittels Raman-Mikrospektroskopie
Quelle ↗Förderer: DFG Exzellenzstrategie Cluster Zeitraum: 01/2023 - 12/2025 Projektleitung: Prof. Dr. rer. nat. Janina Kneipp
Surface-enhanced Raman spectroscopy in liquid biopsy for breast cancer
Quelle ↗Förderer: Horizon Europe: Postdoctoral Fellowship EU (PF-EU) Zeitraum: 10/2023 - 09/2025 Projektleitung: Prof. Dr. rer. nat. Janina Kneipp
Mögliche Industrie-Partner10
Stand: 26.4.2026, 19:48:44 (Top-K=20, Min-Cosine=0.4)
- 134 Treffer85.0%
- Surface-enhanced Raman spectroscopy in liquid biopsy for breast cancerK85.0%
- Surface-enhanced Raman spectroscopy in liquid biopsy for breast cancer
- DYnamic control in hybrid plasmonic NAnopores: road to next generation multiplexed single MOlecule detectionK85.0%
- DYnamic control in hybrid plasmonic NAnopores: road to next generation multiplexed single MOlecule detection
- 134 Treffer85.0%
- Surface-enhanced Raman spectroscopy in liquid biopsy for breast cancerK85.0%
- Surface-enhanced Raman spectroscopy in liquid biopsy for breast cancer
- 56 Treffer60.1%
- Entwicklung von wenig löslichen, homodispers nanoskopischen Metallfluoriden in Zahnzementen, Kompositfüllmaterialien und in Prophylaxepräparaten zum Einsatz im DentalbereichP60.1%
- Entwicklung von wenig löslichen, homodispers nanoskopischen Metallfluoriden in Zahnzementen, Kompositfüllmaterialien und in Prophylaxepräparaten zum Einsatz im Dentalbereich
- 26 Treffer59.5%
- EU: Printed Logic for Applications of Screen Matrix Activation (PLASMAS)P59.5%
- EU: Printed Logic for Applications of Screen Matrix Activation (PLASMAS)
- 24 Treffer59.5%
- EU: Printed Logic for Applications of Screen Matrix Activation (PLASMAS)P59.5%
- EU: Printed Logic for Applications of Screen Matrix Activation (PLASMAS)
- 28 Treffer59.5%
- EU: Printed Logic for Applications of Screen Matrix Activation (PLASMAS)P59.5%
- EU: Printed Logic for Applications of Screen Matrix Activation (PLASMAS)
- 27 Treffer59.5%
- EU: Printed Logic for Applications of Screen Matrix Activation (PLASMAS)P59.5%
- EU: Printed Logic for Applications of Screen Matrix Activation (PLASMAS)
- 29 Treffer59.5%
- EU: Printed Logic for Applications of Screen Matrix Activation (PLASMAS)P59.5%
- EU: Printed Logic for Applications of Screen Matrix Activation (PLASMAS)
- 108 Treffer57.9%
- EU: Monomer Sequence Control in Polymers: Toward Next-Generation Precision Materials (EURO-SEQUENCES)T57.9%
- EU: Monomer Sequence Control in Polymers: Toward Next-Generation Precision Materials (EURO-SEQUENCES)
Publikationen25
Top 25 nach Zitationen — Quelle: OpenAlex (BAAI/bge-m3 embedded für Matching).
ACS Nano · 3655 Zitationen · DOI
The discovery of the enhancement of Raman scattering by molecules adsorbed on nanostructured metal surfaces is a landmark in the history of spectroscopic and analytical techniques. Significant experimental and theoretical effort has been directed toward understanding the surface-enhanced Raman scattering (SERS) effect and demonstrating its potential in various types of ultrasensitive sensing applications in a wide variety of fields. In the 45 years since its discovery, SERS has blossomed into a rich area of research and technology, but additional efforts are still needed before it can be routinely used analytically and in commercial products. In this Review, prominent authors from around the world joined together to summarize the state of the art in understanding and using SERS and to predict what can be expected in the near future in terms of research, applications, and technological development. This Review is dedicated to SERS pioneer and our coauthor, the late Prof. Richard Van Duyne, whom we lost during the preparation of this article.
Chemical Society Reviews · 1063 Zitationen · DOI
Surface enhanced Raman scattering (SERS) at extremely high enhancement level turns the weak inelastic scattering effect of photons on vibrational quantum states into a structurally sensitive single-molecule and nanoscale probe. The effect opens up exciting opportunities for applications of vibrational spectroscopy in biology. The concept of SERS can be extended to two-photon excitation by exploiting surface enhanced hyper-Raman scattering (SEHRS). This critical review introduces the physics behind single-molecule SERS and discusses the capabilities of the effect in bioanalytics (100 references).
Accounts of Chemical Research · 648 Zitationen · DOI
This Account discusses surface-enhanced Raman scattering at extremely high enhancement levels that can occur for molecules attached to silver and gold nanoclusters. Strongly enhanced and highly confined local optical fields enable surface-enhanced Stokes and anti-Stokes Raman spectroscopy of single molecules even under nonresonant excitation conditions as well as extremely large effective cross sections in two-photon excited Raman spectroscopy. The ability for very sensitive and spatially confined molecular structural probing makes gold and silver nanoclusters very promising tools for studies of small structures in biological materials, such as cellular compartments.
Angewandte Chemie International Edition · 561 Zitationen · DOI
Experimental results obtained in different laboratories world-wide by researchers using surface-enhanced Raman scattering (SERS) can differ significantly. We, an international team of scientists with long-standing expertise in SERS, address this issue from our perspective by presenting considerations on reliable and quantitative SERS. The central idea of this joint effort is to highlight key parameters and pitfalls that are often encountered in the literature. To that end, we provide here a series of recommendations on: a) the characterization of solid and colloidal SERS substrates by correlative electron and optical microscopy and spectroscopy, b) on the determination of the SERS enhancement factor (EF), including suitable Raman reporter/probe molecules, and finally on c) good analytical practice. We hope that both newcomers and specialists will benefit from these recommendations to increase the inter-laboratory comparability of experimental SERS results and further establish SERS as an analytical tool.
Nano Letters · 469 Zitationen · DOI
Surface-enhanced Raman (SERS) signatures were measured from single living cells at different times after the uptake of gold nanoparticles. The spectra are indicative of chemical changes in the environment of the nanostructures over time. The increase of the SERS signal strength and parallel TEM studies indicate the formation of nanoaggregates providing optimum SERS enhancement for ultrasensitive probing inside the endosomal compartment. The results have implications for medical and biotechnology applications of SERS nanosensors in cells.
Scientific Reports · 358 Zitationen · DOI
MALDI time-of-flight mass spectrometry (MALDI-TOF MS) has become a widely used tool for the classification of biological samples. The complex chemical composition of pollen grains leads to highly specific, fingerprint-like mass spectra, with respect to the pollen species. Beyond the species-specific composition, the variances in pollen chemistry can be hierarchically structured, including the level of different populations, of environmental conditions or different genotypes. We demonstrate here the sensitivity of MALDI-TOF MS regarding the adaption of the chemical composition of three Poaceae (grass) pollen for different populations of parent plants by analyzing the mass spectra with partial least squares discriminant analysis (PLS-DA) and principal component analysis (PCA). Thereby, variances in species, population and specific growth conditions of the plants were observed simultaneously. In particular, the chemical pattern revealed by the MALDI spectra enabled discrimination of the different populations of one species. Specifically, the role of environmental changes and their effect on the pollen chemistry of three different grass species is discussed. Analysis of the group formation within the respective populations showed a varying influence of plant genotype on the classification, depending on the species, and permits conclusions regarding the respective rigidity or plasticity towards environmental changes.
Nano Letters · 325 Zitationen · DOI
We demonstrate spatially resolved probing and imaging of pH in live cells by mobile and biocompatible nanosensors using surface-enhanced Raman scattering (SERS) of 4-mercaptobenzoic acid (pMBA) on gold nanoaggregates. Moreover, we also show that this concept of pH nanosensors can be extended to two-photon excitation by using surface-enhanced hyper-Raman scattering (SEHRS). In addition to the advantages of two-photon excitation, the SEHRS sensor enables measurements over a wide pH range without the use of multiple probes.
Nanomedicine Nanotechnology Biology and Medicine · 286 Zitationen · DOI
Chemical Society Reviews · 255 Zitationen · DOI
Surface-enhanced Raman spectroscopy (SERS) has evolved significantly over fifty years into a powerful analytical technique. This review aims to achieve five main goals. (1) Providing a comprehensive history of SERS's discovery, its experimental and theoretical foundations, its connections to advances in nanoscience and plasmonics, and highlighting collective contributions of key pioneers. (2) Classifying four pivotal phases from the view of innovative methodologies in the fifty-year progression: initial development (mid-1970s to mid-1980s), downturn (mid-1980s to mid-1990s), nano-driven transformation (mid-1990s to mid-2010s), and recent boom (mid-2010s onwards). (3) Illuminating the entire journey and framework of SERS and its family members such as tip-enhanced Raman spectroscopy (TERS) and shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS) and highlighting the trajectory. (4) Emphasizing the importance of innovative methods to overcome developmental bottlenecks, thereby expanding the material, morphology, and molecule generalities to leverage SERS as a versatile technique for broad applications. (5) Extracting the invaluable spirit of groundbreaking discovery and perseverant innovations from the pioneers and trailblazers. These key inspirations include proactively embracing and leveraging emerging scientific technologies, fostering interdisciplinary cooperation to transform the impossible into reality, and persistently searching to break bottlenecks even during low-tide periods, as luck is what happens when preparation meets opportunity.
Analytical Chemistry · 251 Zitationen · DOI
We report surface-enhanced Raman scattering (SERS) studies on indocyanine green (ICG) on colloidal silver and gold and demonstrate a novel optical probe for applications in living cells. In addition to its own detection by the characteristic ICG SERS signatures, the ICG gold nanoprobe delivers spatially localized chemical information from its biological environment by employing SERS in the local optical fields of the gold nanoparticles. The probe offers the potential to increase the spectral specificity and selectivity of current chemical characterization approaches of living cells and biomaterials based on vibrational information.
The Journal of Physical Chemistry C · 209 Zitationen · DOI
Using picosecond excitation at 1064 nm, surface-enhanced hyper-Raman scattering (SEHRS) spectra of the nucleobases adenine, guanine, cytosine, thymine, and uracil with two different types of silver nanoparticles were obtained. Comparing the SEHRS spectra with SERS data from the identical samples excited at 532 nm and with known infrared spectra, the major bands in the spectra are assigned. Due to the different selection rules for the one- and two-photon excited Raman scattering, we observe strong variation in relative signal strengths of many molecular vibrations obtained in SEHRS and SERS spectra. The two-photon excited spectra of the nucleobases are found to be very sensitive with respect to molecule-nanoparticle interactions. Using both the SEHRS and SERS data, a comprehensive vibrational characterization of the interaction of nucleobases with silver nanostructures can be achieved.
The Journal of Physical Chemistry C · 206 Zitationen · DOI
The surface enhanced Raman scattering (SERS) spectrum of a reporter molecule attached to gold or silver nanostructures, which is pH-sensitive, can deliver information on the local pH in the environment of the nanostructure. Here, we demonstrate the use of a mobile SERS nanosensor made from gold nanaoaggregates and 4-mercaptobenzoic acid (pMBA) attached as a reporter for monitoring changes in local pH of the cellular compartments of living NIH/3T3 cells. We show that SERS nanosensors enable the dynamics of local pH in individual live cells to be followed at subendosomal resolution in a timeline of cellular processes. This information is of basic interest for a better understanding of a broad range of physiological and metabolic processes as well as for a number of biotechnological applications.
Analytical Chemistry · 199 Zitationen · DOI
Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) was utilized for spatially resolved bioimaging of the distribution of silver and gold nanoparticles in individual fibroblast cells upon different incubation experiments. High spatial resolution was achieved by optimization of scan speed, ablation frequency, and laser energy. Nanoparticles are visualized with respect to cellular substructures and are found to accumulate in the perinuclear region with increasing incubation time. On the basis of matrix-matched calibration, we developed a method for quantification of the number of metal nanoparticles at the single-cell level. The results provide insight into nanoparticle/cell interactions and have implications for the development of analytical methods in tissue diagnostics and therapeutics.
Characterizing the Kinetics of Nanoparticle‐Catalyzed Reactions by Surface‐Enhanced Raman Scattering
2012Angewandte Chemie International Edition · 171 Zitationen · DOI
Separate gold and platinum nanoparticles simultaneously immobilized on a glass surface were used to study the kinetics of a catalytic reaction directly. Owing to the proximity of the platinum and gold nanoparticles, the analyte molecules can interact with the platinum nanoparticles whilst they reside in the local optical fields of the gold nanoparticles. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Journal of Raman Spectroscopy · 165 Zitationen · DOI
Abstract Monodisperse, citrate‐stabilized gold nanoparticles of sizes ranging from 15 to 40 nm were synthesized and characterized by small angle X‐ray scattering and UV‐vis experiments. Identical surface properties of nanoparticles of different sizes to avoid variation in the chemical surface‐enhanced Raman scattering (SERS) enhancement, as well as selection of experimental conditions so that no aggregation took place, enabled the investigation of enhancement of individual nanospheres. Enhancement factors (EFs) for SERS were determined using the dye crystal violet (CV). EFs for individual gold nanospheres ranged from 10 2 to 10 3 , in agreement with theoretical predictions. An increase of the EFs of individual spheres with size can be correlated to changes in the extinction spectra of nanoparticle solutions. This confirms that the increase in enhancement with increasing size results from an increase in electromagnetic enhancement. Beyond this dependence of EFs of isolated gold spheres on their size, EFs were shown to vary with analyte concentration as a result of analyte‐induced aggregation. This has implications for the application of nanoparticle solutions as SERS substrates in quantitative analytical tasks. Copyright © 2011 John Wiley & Sons, Ltd.
Journal of Raman Spectroscopy · 155 Zitationen · DOI
Abstract During surface‐enhanced Raman scattering (SERS), molecules exhibit a significant increase in their Raman signals when attached, or in very close vicinity, to gold or silver nanostructures. This effect is exploited as the basis of a new class of optical labels. Here we demonstrate robust and sensitive SERS labels as probes for imaging live cells. These hybrid labels consist of gold nanoparticles with Rose Bengal or Crystal Violet attached as reporter molecules. These new labels are stable and nontoxic, do not suffer from photobleaching, and can be excited at any excitation wavelength, even in the near infrared. SERS labels can be detected and imaged through the specific Raman signatures of the reporters. In addition, surface‐enhanced Raman spectroscopy in the local optical fields of the gold nanoparticles also provides sensitive information on the immediate molecular environment of the label in the cell and allows imaging of the native constituents of the cell. This is demonstrated by images based on a characteristic Raman line of the reporter as well as by displaying lipids based on the SERS signal of the CH deformation/bending modes at ∼1470 cm −1 . Copyright © 2008 John Wiley & Sons, Ltd.
Frontiers in Chemistry · 151 Zitationen · DOI
The collection of surface-enhanced Raman scattering (SERS) spectra of proteins and other biomolecules in complex biological samples such as animal cells has been achieved with gold nanoparticles that are introduced to the sample. As a model for such a situation, SERS spectra were measured in protein solutions using gold nanoparticles in the absence of aggregating agents, allowing for the free formation of a protein corona. The SERS spectra indicate a varied interaction of the protein molecule with the gold nanoparticles, depending on protein concentration. The concentration-dependent optical properties of the formed agglomerates result in strong variation in SERS enhancement. At protein concentrations that correspond to those inside cells, SERS signals are found to be very low. The results suggest that in living cells the successful collection of SERS spectra must be due to the positioning of the aggregates rather than the crowded biomolecular environment inside the cells. Experiments with DNA suggest the suitability of the applied sample preparation approach for an improved understanding of SERS nanoprobes and nanoparticle-biomolecule interactions in general.
Nature Reviews Methods Primers · 146 Zitationen · DOI
Two-photon vibrational spectroscopy for biosciences based on surface-enhanced hyper-Raman scattering
2006Proceedings of the National Academy of Sciences · 145 Zitationen · DOI
Two-photon excitation is gaining rapidly in interest and significance in spectroscopy and microscopy. Here we introduce a new approach that suggests versatile optical labels suitable for both one- and two-photon excitation and also two-photon-excited ultrasensitive, nondestructive chemical probing. The underlying spectroscopic effect is the incoherent inelastic scattering of two photons on the vibrational quantum states called hyper-Raman scattering (HRS). The rather weak effect can be strengthened greatly if HRS takes place in the local optical fields of gold and silver nanostructures. This so-called surface-enhanced HRS (SEHRS) is the two-photon analogue to surface-enhanced Raman scattering (SERS). SEHRS provides structurally sensitive vibrational information complementary to those obtained by SERS. SEHRS combines the advantages of two-photon spectroscopy with the structural information of vibrational spectroscopy and the high-sensitivity and nanometer-scale local confinement of plasmonics-based spectroscopy. We infer effective two-photon cross-sections for SEHRS on the order of 10(-46) to 10(-45) cm4 x s, similar to or higher than the best "action" cross-sections (product of the two-photon absorption cross-section and fluorescence quantum yield) for two-photon fluorescence, and we demonstrate HRS on biological structures such as single cells after incubation with gold nanoparticles.
Surface-Enhanced Raman Scattering Hybrid Nanoprobe Multiplexing and Imaging in Biological Systems
2010ACS Nano · 135 Zitationen · DOI
Surface-enhanced Raman scattering (SERS) labels and probes consisting of gold and silver nanoaggregates and attached reporter molecules can be identified by the Raman signature of the reporter molecule. At the same time, SERS hybrid probes deliver sensitive molecular structural information on their nanoenvironment. Here we demonstrate full exploitation of the multifunctional and multiplexing capabilities inherent to such nanoprobes by applying cluster methods and principal components approaches for discrimination beyond the visual inspection of individual spectra that has been practiced so far. The reported results indicate that fast, multivariate evaluation of whole sets of multiple probes is feasible. Spectra of five different reporters were shown to be separable by hierarchical clustering and by principal components analysis (PCA). In a duplex imaging approach in live cells, hierarchical cluster analysis, K-means clustering, and PCA were used for imaging the positions of different types of SERS probes along with the spectral information from cellular constituents. Parallel to cellular imaging experiments, cytotoxicity of the SERS hybrid probes containing aromatic thiols as reporters is assessed. The reported results suggest multiplexing applications of the nontoxic SERS nanoprobes in high density sensing and imaging in complex biological structures.
Analytical and Bioanalytical Chemistry · 134 Zitationen · DOI
Analytical Chemistry · 133 Zitationen · DOI
We report on the in situ characterization of tree pollen molecular composition based on Raman spectroscopy. Different from purification-based analysis, the nondestructive approach allows (i) to analyze various classes of molecules simultaneously at microscopic resolution and (ii) to acquire fingerprint-like chemical information that was used for the classification of pollen from different species. Hierarchical cluster analysis of spectra from fresh pollen samples of 15 species partly related at the genus level and family level indicates separation of species based on the complete Raman spectral signature and yields classification in accord with biological systematics. The results have implications for the further elucidation of pollen biochemistry and also for the development of chemistry-based online pollen identification methods.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 118 Zitationen · DOI
Physical Chemistry Chemical Physics · 109 Zitationen · DOI
The interaction of nanoparticles with hemoglobin (Hb), a major constituent of red blood cells, is important in nanotoxicity research. We report SERS spectra of Hb using gold and silver nanoparticles at very small nanoparticle : Hb molecule ratios, that is, under conditions relevant for SERS-based nanotoxicity experiments with red blood cells at high sensitivity. We show that the structural information obtained from the experiment is highly dependent on the type of SERS substrate and the conditions under which the interaction of nanoparticles with Hb molecules takes place. In experiments with isolated red blood cells, we demonstrate that the dependence of the spectra on the type of nanoparticle used as the SERS substrate extends to whole red blood cells and red blood cell components. Regarding the applicability of SERS to red blood cells in vivo, evidence is provided that the molecular information contained in the spectra is highly dependent on the material and size of the nanoparticles. The results indicate specific interactions of gold and silver nanoparticles with Hb and the red blood cell membrane, and reflect the hemolytic activity of silver nanoparticles. The results of this study help improve our understanding of the interactions of silver and gold nanoparticles with red blood cells.
Analytical and Bioanalytical Chemistry · 109 Zitationen · DOI
Kooperationen20
Bestätigte Forscher↔Partner-Paare aus HU-FIS — Gold-Standard-Positive für das Matching.
DYnamic control in hybrid plasmonic NAnopores: road to next generation multiplexed single MOlecule detection
other
Silica incorporation into newly synthesized cell walls and its effects on physiological properties of plant cells
other
DYnamic control in hybrid plasmonic NAnopores: road to next generation multiplexed single MOlecule detection
other
EXC 2008: Unifying Systems in Catalysis (UniSysCat)
university
EXC 2008: Unifying Systems in Catalysis (UniSysCat)
university
EXC 2008: Unifying Systems in Catalysis (UniSysCat)
other
Silica incorporation into newly synthesized cell walls and its effects on physiological properties of plant cells
university
Größenskalen in der molekularen Bildgebung verbinden: Eine Synchrotron-Mikroskopie-Station für räumliche, zeitliche und polarisationsaufgelöste Schwingungsspektroskopie
other
Surface-enhanced Raman spectroscopy in liquid biopsy for breast cancer
other
Surface-enhanced Raman spectroscopy in liquid biopsy for breast cancer
other
DYnamic control in hybrid plasmonic NAnopores: road to next generation multiplexed single MOlecule detection
other
EXC 2008: Unifying Systems in Catalysis (UniSysCat)
other
EXC 2008: Unifying Systems in Catalysis (UniSysCat)
other
Silica incorporation into newly synthesized cell walls and its effects on physiological properties of plant cells
university
DYnamic control in hybrid plasmonic NAnopores: road to next generation multiplexed single MOlecule detection
university
Technische Universität Nanyang
Surface-enhanced Raman spectroscopy in liquid biopsy for breast cancer
university
DYnamic control in hybrid plasmonic NAnopores: road to next generation multiplexed single MOlecule detection
university
DYnamic control in hybrid plasmonic NAnopores: road to next generation multiplexed single MOlecule detection
university
DYnamic control in hybrid plasmonic NAnopores: road to next generation multiplexed single MOlecule detection
university
EXC 2008: Unifying Systems in Catalysis (UniSysCat)
university
Stammdaten
Identität, Organisation und Kontakt aus HU-FIS.
- Name
- Prof. Dr. rer. nat. Janina Kneipp
- Titel
- Prof. Dr. rer. nat.
- Fakultät
- Mathematisch-Naturwissenschaftliche Fakultät
- Institut
- Institut für Chemie
- Arbeitsgruppe
- Physikalische Chemie
- Telefon
- +49 30 2093-82632
- HU-FIS-Profil
- Quelle ↗
- Zuletzt gescrapt
- 26.4.2026, 01:07:39