Bibliographies thématiques / Cell culture techniques – laboratory manuals

Littérature scientifique sur le sujet « Cell culture techniques – laboratory manuals »

Auteur : Grafiati
Publié le 26 juillet 2024
Mis à jour le 26 juillet 2024

Créez une référence correcte selon les styles APA, MLA, Chicago, Harvard et plusieurs autres

Choisissez une source :

Sommaire

Consultez les listes thématiques d’articles de revues, de livres, de thèses, de rapports de conférences et d’autres sources académiques sur le sujet « Cell culture techniques – laboratory manuals ».

À côté de chaque source dans la liste de références il y a un bouton « Ajouter à la bibliographie ». Cliquez sur ce bouton, et nous générerons automatiquement la référence bibliographique pour la source choisie selon votre style de citation préféré : APA, MLA, Harvard, Vancouver, Chicago, etc.

Vous pouvez aussi télécharger le texte intégral de la publication scolaire au format pdf et consulter son résumé en ligne lorsque ces informations sont inclues dans les métadonnées.

Articles de revues sur le sujet "Cell culture techniques – laboratory manuals"

1

Clothier, Richard H. « Book Review : Culture of Animals Cells : Manual of Basic Technique — Third Edition ». Alternatives to Laboratory Animals 23, no 1 (janvier 1995) : 161. http://dx.doi.org/10.1177/026119299502300121.

Texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
2

Hulme, Lesley. « Book Review : Culture of Animal Cells : A Manual of Basic Technique— 2Nd Edition ». Alternatives to Laboratory Animals 16, no 1 (septembre 1988) : 97. http://dx.doi.org/10.1177/026119298801600119.

Texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
3

Braylan, Raul C., et Elaine Kay Jordan. « Rapid and Simple Procedure For Isolation and Concentration Of Human Megakaryocytes From Marrow Aspirates ». Blood 122, no 21 (15 novembre 2013) : 5269. http://dx.doi.org/10.1182/blood.v122.21.5269.5269.

Texte intégral
Résumé :
Abstract Background Numerical and morphologic abnormalities of megakaryocytes (MKs) are present in a variety of primary or secondary bone marrow (BM) disorders such as myeloproliferative neoplasms, myelodysplastic syndromes or ITP. Currently, these changes are assessed exclusively on microscopic preparations of marrow aspirates and biopsies and are used as criteria for disease diagnosis, classification and therapy monitoring despite the inherent subjectivity of microscopic evaluations. In contrast to other cells, adequate studies of freshly isolated MKs have proven difficult because of the relative rarity of these cells in the BM (∼0.05% of total nucleated cells) and separation techniques such as density gradients, magnetic beads, centrifugal elutriation or fluorescence activated cell sorting are labor-intensive, time-consuming or costly. The primary means for studying MKs is based on the isolation of progenitors primed with cytokines to differentiate in culture. While extremely valuable, these techniques are not directly translatable to the routine clinical arena for assessing MK pathology in human BM. Mature marrow MKs are large, polyploid cells whose size distribution overlaps minimally with that of all other marrow cells. This distinct size threshold is a discriminatory parameter for MK isolation. Thus, we developed a simple and inexpensive manual mesh filtration method for separation of MKs that allows a rapid and easy, size-based concentration and purification of these cells. Methods We examined 15 discarded anonymized BM aspirate samples suitable for our analysis. These samples were from patients with a variety of hematologic disorders originally submitted to our laboratory for evaluation. Sample age ranged from 1-4 days (mean 1.5 days). Samples were diluted with heparin/albumin-containing buffered saline solution. The cell suspensions were first filtered through a 70µm filter to remove large BM stromal particles and then twice (by gravity) through 9mm-diameter wetted 8 µm nylon filters placed in a simple plastic holder. This filtration procedure allowed the retention of MKs and removal of smaller cells. The MK-rich suspension was collected by rinsing and flushing the filters with the buffered solution. On average, the procedure only lasted 15 minutes. The pre-filtered, 8 µm filter-retained, and effluent cell suspensions collected were stained with an FITC-anti CD61 or PE-anti CD41a antibody [Becton Dickinson (BD)] to label MKs, concurrently with the cell permeable DNA-binding DRAQ5 (Cell Signaling Technology) to identify all nucleated cells. Final cell viability was assessed by C12Resazurin (Molecular probes). Cell analysis was performed by flow cytometry (FCM) using a CANTO II flow cytometer (BD). Absolute MK enumeration was performed using the Flow Cytometry Absolute Count Standard beads (Bangs). MK enrichment efficiency was expressed as the percentage of MKs of all nucleated cells determined by FCM. No cell lysing, fixation or centrifugation was used at any step of the MK separation procedure. Results The median (range) volume of the BM aspirate samples used in this study was 0.54 (0.24-1.99) mL. MKs were identified by FCM on the basis of their large size, expression of platelet-associated antigens and DNA ploidy levels. The median (range) MK recovery was 31 (14-100) % of the original number of MKs and the yield was 9,882 (1,519-49,921) MKs per mL of BM aspirate. The median (range) fraction of MKs among all nucleated cells after filtration was 39 (14-68) %, representing a 904 (439-3029)-fold MK enrichment. The MK viability after filtration was near 100%. Conclusions This simple, gentle, rapid and inexpensive isolation and concentration method results in a MK recovery and purification that is comparable or better than other more elaborate techniques. Despite the inherent heterogeneity of the samples used, we obtained a reasonably good recovery of MKs per mL of marrow aspirate and more than 900-fold median MK concentration. The yield and level of purification of freshly isolated MKs obtained by this simple procedure may be useful in studies of a variety of primary or secondary marrow disorders. In particular, it should facilitate the application of analytical methods such as flow cytometry or in situ hybridization, and even be useful for biochemical or molecular testing that require adequate cell representation and purity. Disclosures: No relevant conflicts of interest to declare.
Styles APA, Harvard, Vancouver, ISO, etc.
4

Hidayat, Nurul, Mega Novia Putri et Ronal Kurniawan. « Nannochloropsis sp phytoplankton culture technique laboratory scale ». South East Asian Marine Sciences Journal 1, no 2 (15 mars 2024) : 73–76. http://dx.doi.org/10.61761/seamas.1.2.73-76.

Texte intégral
Résumé :
Nannochloropsis sp is a phytoplankton often used in marine fish hatchery activities as feed for the mass production of rotifers, and its availability is very much needed for rearing marine fish larvae. This activity aims to study pure culture techniques for Nannochloropsis sp on a laboratory scale. The method used is a literature study method and a direct practical method regarding Nannochloropsis sp phytoplankton culture techniques laboratory scale and conducted interviews with employees at the BPBL Batam Phytoplankton Live Food Production Unit Laboratory. Based on observations, it was found that the peak growth or optimum cell density of Nannochloropsis sp. occurred on the sixth day in a 1000 mL Erlenmeyer, namely 60.95 - 62.10 million cells/mL with an initial density of 10.15 - 10.55 million cells/mL and in a 2000 mL Erlenmeyer, namely 58.75 - 60, 25 million cells/mL with an initial density of 8.25 – 8.45 million cells/mL.
Styles APA, Harvard, Vancouver, ISO, etc.
5

Lewis, Jennifer R., Mark S. Kotur, Omar Butt, Sumant Kulcarni, Alyssa A. Riley, Nick Ferrell, Kathryn D. Sullivan et Mauro Ferrari. « Biotechnology Apprenticeship for Secondary-Level Students : Teaching Advanced Cell Culture Techniques for Research ». Cell Biology Education 1, no 1 (mars 2002) : 26–42. http://dx.doi.org/10.1187/cbe.02-02-0003.

Texte intégral
Résumé :
The purpose of this article is to discuss small-group apprenticeships (SGAs) as a method to instruct cell culture techniques to high school participants. The study aimed to teach cell culture practices and to introduce advanced imaging techniques to solve various biomedical engineering problems. Participants designed and completed experiments using both flow cytometry and laser scanning cytometry during the 1-month summer apprenticeship. In addition to effectively and efficiently teaching cell biology laboratory techniques, this course design provided an opportunity for research training, career exploration, and mentoring. Students participated in active research projects, working with a skilled interdisciplinary team of researchers in a large research institution with access to state-of-the-art instrumentation. The instructors, composed of graduate students, laboratory managers, and principal investigators, worked well together to present a real and worthwhile research experience. The students enjoyed learning cell culture techniques while contributing to active research projects. The institution's researchers were equally enthusiastic to instruct and serve as mentors. In this article, we clarify and illuminate the value of small-group laboratory apprenticeships to the institution and the students by presenting the results and experiences of seven middle and high school participants and their instructors.
Styles APA, Harvard, Vancouver, ISO, etc.
6

Bleotu, Coralia, Carmen Diaconu, Mihaela Chivu, Irina Alexiu, Simona Ruta et Costin Cernescu. « Evaluation of TV cell line viral susceptibility using conventional cell culture techniques ». Open Medicine 1, no 1 (1 mars 2006) : 12–22. http://dx.doi.org/10.2478/s11536-006-0007-x.

Texte intégral
Résumé :
AbstractDespite the fact that a lot of methods have been developed for rapid virus detection, classic cell culture is still “the golden standard”. The range of viruses that can be isolated and cultured in cell line systems is often limited by the susceptibility of cells to support viral replication. Since the primary cell culture, the best cellular system available to support replication of a large number of viruses, is very expensive and diffcult to obtain, cell lines, which are easier to manipulate, are commonly used for virus growth and isolation.In two previous papers we described the TV cell line initiated by our team from a laryngeal tumor, which harbors human papillomavirus (HPV) gene sequences. In this paper we analyze its capacity to support virus replication. Depending on the virus, different cytopathic effects were produced. Comparison of viral effect observed on this cell line with the effect obtained on other cell lines has been performed. This cell line might be used in the clinical virology laboratory for virus isolation.
Styles APA, Harvard, Vancouver, ISO, etc.
7

Ciapetti, Gabriela, Elisabetta Cenni, Daniela Cavedagna, Loredana Pratelli et Arturo Pizzoferrato. « Cell Culture Methods to Evaluate the Biocompatibility of Implant Materials ». Alternatives to Laboratory Animals 20, no 1 (janvier 1992) : 52–60. http://dx.doi.org/10.1177/026119299202000107.

Texte intégral
Résumé :
Cell culture techniques are usually used in the field of biomaterials research and development in order to detect toxic components. Morphological assays are the most widely used methods and give the very first information about the biological compatibility of materials. Cell function assays give more quantitative data, but the comparison of data between different laboratories is difficult. Some of the cell culture methods that are used for biocompatibility studies are described briefly here, and results from our laboratory are reported. Despite some inherent limitations of the cell culture techniques, they are an accurate and reliable method of predicting the biological compatibility of materials to be implanted in vivo.
Styles APA, Harvard, Vancouver, ISO, etc.
8

Marion, Rebecca E., Grant E. Gardner et Lisa D. Parks. « Multiweek cell culture project for use in upper-level biology laboratories ». Advances in Physiology Education 36, no 2 (juin 2012) : 154–57. http://dx.doi.org/10.1152/advan.00080.2011.

Texte intégral
Résumé :
This article describes a laboratory protocol for a multiweek project piloted in a new upper-level biology laboratory (BIO 426) using cell culture techniques. Human embryonic kidney-293 cells were used, and several culture media and supplements were identified for students to design their own experiments. Treatments included amino acids, EGF, caffeine, epinephrine, heavy metals, and FBS. Students researched primary literature to determine their experimental variables, made their own solutions, and treated their cells over a period of 2 wk. Before this, a sterile technique laboratory was developed to teach students how to work with the cells and minimize contamination. Students designed their experiments, mixed their solutions, seeded their cells, and treated them with their control and experimental media. Students had the choice of manipulating a number of variables, including incubation times, exposure to treatment media, and temperature. At the end of the experiment, students observed the effects of their treatment, harvested and dyed their cells, counted relative cell numbers in control and treatment flasks, and determined the ratio of living to dead cells using a hemocytometer. At the conclusion of the experiment, students presented their findings in a poster presentation. This laboratory can be expanded or adapted to include additional cell lines and treatments. The ability to design and implement their own experiments has been shown to increase student engagement in the biology-related laboratory activities as well as develop the critical thinking skills needed for independent research.
Styles APA, Harvard, Vancouver, ISO, etc.
9

Shyam, Rohin, L. Reddy et Arunkumar Palaniappan. « Fabrication and Characterization Techniques of In Vitro 3D Tissue Models ». International Journal of Molecular Sciences 24, no 3 (18 janvier 2023) : 1912. http://dx.doi.org/10.3390/ijms24031912.

Texte intégral
Résumé :
The culturing of cells in the laboratory under controlled conditions has always been crucial for the advancement of scientific research. Cell-based assays have played an important role in providing simple, fast, accurate, and cost-effective methods in drug discovery, disease modeling, and tissue engineering while mitigating reliance on cost-intensive and ethically challenging animal studies. The techniques involved in culturing cells are critical as results are based on cellular response to drugs, cellular cues, external stimuli, and human physiology. In order to establish in vitro cultures, cells are either isolated from normal or diseased tissue and allowed to grow in two or three dimensions. Two-dimensional (2D) cell culture methods involve the proliferation of cells on flat rigid surfaces resulting in a monolayer culture, while in three-dimensional (3D) cell cultures, the additional dimension provides a more accurate representation of the tissue milieu. In this review, we discuss the various methods involved in the development of 3D cell culture systems emphasizing the differences between 2D and 3D systems and methods involved in the recapitulation of the organ-specific 3D microenvironment. In addition, we discuss the latest developments in 3D tissue model fabrication techniques, microfluidics-based organ-on-a-chip, and imaging as a characterization technique for 3D tissue models.
Styles APA, Harvard, Vancouver, ISO, etc.
10

Malovrh, Tadej, et Peter Hostnik. « Diagnostics procedures in rabies ». Veterinarski glasnik 59, no 1-2 (2005) : 99–105. http://dx.doi.org/10.2298/vetgl0502099m.

Texte intégral
Résumé :
Rabies is a major zoonosis for which diagnostic techniques can only be performed in the laboratory. Laboratory techniques are preferably oriented on tissue removed from the cranium: hippocampus (Ammon's horn), cerebellum and the medulla oblongata or tissue liquids. Clinical observation may only lead to a suspicion of rabies. The only way to perform a reliable diagnosis of the disease is to identify the virus or some of its specific components using laboratory tests such as histological identification of characteristic cell lesions, immunochemical identification of rabies virus antigen and virus isolation. Serological tests are rarely used in epidemiological surveys but much more frequently in control of the vaccination programs (e.g. oral vaccination). Most commonly used serological tests are the virus neutralization test on cell culture (FAVN), virus neutralization in mice and ELISA.
Styles APA, Harvard, Vancouver, ISO, etc.
Plus de sources

Livres sur le sujet "Cell culture techniques – laboratory manuals"

1

M, Clynes, dir. Animal cell culture techniques. Berlin : Springer, 1998.

Trouver le texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
2

1939-, Rae Ian F., dir. General techniques of cell culture. Cambridge : Cambridge University Press, 1997.

Trouver le texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
3

Mitry, Ragai R., et Robin D. Hughes. Human cell culture protocols. 3e éd. New York : Humana Press, 2012.

Trouver le texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
4

Joanna, Picot, dir. Human cell culture protocols. 2e éd. Totowa, N.J : Humana Press, 2005.

Trouver le texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
5

D, Helgason Cheryl, et Miller Cindy L, dir. Basic cell culture protocols. 3e éd. Totowa, N.J : Humana Press, 2005.

Trouver le texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
6

Loyola-Vargas, Victor M., et Neftalí Ochoa-Alejo. Plant cell culture protocols. 3e éd. New York : Springer, 2012.

Trouver le texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
7

Cree, Ian A. Cancer cell culture : Methods and protocols. 2e éd. Totowa, N.J : Humana Press, 2011.

Trouver le texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
8

Haycock, John W. 3D cell culture : Methods and protocols. New York : Humana Press/Springer, 2011.

Trouver le texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
9

Haycock, John W. 3D cell culture : Methods and protocols. New York : Humana Press/Springer, 2011.

Trouver le texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
10

Randell, Scott H., et M. Leslie Fulcher. Epithelial cell culture protocols. 2e éd. New York : Humana Press, 2012.

Trouver le texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
Plus de sources

Chapitres de livres sur le sujet "Cell culture techniques – laboratory manuals"

1

Jain, Anvi, Aaru Gulati, Khushi R. Mittal et Shalini Mani. « Cell Culture Laboratory ». Dans Techniques in Life Science and Biomedicine for the Non-Expert, 11–52. Cham : Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-19485-6_2.

Texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
2

Ganesh, Goutham V., Kannan Harithpriya, Dhamodharan Umapathy, Md Enamul Hoque et K. M. Ramkumar. « Laboratory Safety ». Dans Advanced Mammalian Cell Culture Techniques, 11–14. Boca Raton : CRC Press, 2023. http://dx.doi.org/10.1201/9781003397755-4.

Texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
3

Seidman, Lisa A. « Common Calculations Relating to Animal Cell Culture Techniques ». Dans Basic Laboratory Calculations for Biotechnology, 391–412. 2e éd. Boca Raton : CRC Press, 2021. http://dx.doi.org/10.1201/9780429282744-26.

Texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
4

Mani, Shalini. « Managing Sterility in Animal Cell Culture Laboratory ». Dans Techniques in Life Science and Biomedicine for the Non-Expert, 65–75. Cham : Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-19485-6_4.

Texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
5

Yukta, Kumari, Mansi Agarwal, Mekhla Pandey, Khushi Mittal, Vidushi Srivastava et Shalini Mani. « Good Laboratory Practices in Animal Cell Culture Laboratory and Biosafety Measures ». Dans Techniques in Life Science and Biomedicine for the Non-Expert, 53–64. Cham : Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-19485-6_3.

Texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
6

« Introduction to the Cell Culture Laboratory ». Dans Manuals in Biomedical Research, 11–22. WORLD SCIENTIFIC, 2010. http://dx.doi.org/10.1142/9789812834782_0002.

Texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
7

« Introduction to the Cell Culture Laboratory ». Dans Manuals in Biomedical Research, 11–22. WORLD SCIENTIFIC, 2004. http://dx.doi.org/10.1142/9789812791122_0002.

Texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
8

« Reagents and Techniques for Cell Culture ». Dans Manuals in Biomedical Research, 97–126. WORLD SCIENTIFIC, 2010. http://dx.doi.org/10.1142/9789812834782_0004.

Texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
9

« Reagents and Techniques for Cell Culture ». Dans Manuals in Biomedical Research, 75–136. WORLD SCIENTIFIC, 2004. http://dx.doi.org/10.1142/9789812791122_0004.

Texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.
10

Jiabei, Tong, Thilakavathy Karuppiah, Sun Zhong, Akon Higuchi et Suresh Kumar Subbiah. « Protocols in stem cell culture ». Dans Stem Cell Laboratory Techniques, 41–69. Elsevier, 2023. http://dx.doi.org/10.1016/b978-0-12-823729-8.00006-3.

Texte intégral
Styles APA, Harvard, Vancouver, ISO, etc.

Actes de conférences sur le sujet "Cell culture techniques – laboratory manuals"

1

Zavrel, Erik A., Michael L. Shuler et Xiling Shen. « A Simple Aspect Ratio Dependent Method of Patterning Microwells for Selective Cell Attachment ». Dans 2018 Design of Medical Devices Conference. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/dmd2018-6811.

Texte intégral
Résumé :
3-D culture has been shown to provide cells with a more physiologically authentic environment than traditional 2-D (planar) culture [1, 2]. 3-D cues allow cells to exhibit more realistic functions and behaviors, e.g., adhesion, spreading, migration, metabolic activity, and differentiation. Knowledge of changes in cell morphology, mechanics, and mobility in response to geometrical cues and topological stimuli is important for understanding normal and pathological cell development [3]. Microfabrication provides unique in vitro approaches to recapitulating in vivo conditions due to the ability to precisely control the cellular microenvironment [4, 5]. Microwell arrays have emerged as robust alternatives to traditional 2D cell culture substrates as they are relatively simple and compatible with existing laboratory techniques and instrumentation [6, 7]. In particular, microwells have been adopted as a biomimetic approach to modeling the unique micro-architecture of the epithelial lining of the gastrointestinal (GI) tract [8–10]. The inner (lumen-facing) surface of the intestine has a convoluted topography consisting of finger-like projections (villi) with deep well-like invaginations (crypts) between them. The dimensions of villi and crypts are on the order of hundreds of microns (100–700 μm in height and 50–250 μm in diameter) [11]. While microwells have proven important in the development of physiologically realistic in vitro models of human intestine, existing methods of ensuring their surface is suitable for cell culture are lacking. Sometimes it is desirable to selectively seed cells within microwells and confine or restrict them to the microwells in which they are seeded. Existing methods of patterning microwells for cell attachment either lack selectivity, meaning cells can adhere and migrate anywhere on the microwell array, i.e., inside microwells or outside of them, or necessitate sophisticated techniques such as micro-contact printing, which requires precise alignment and control to selectively pattern the bottoms of microwells for cell attachment [12, 13].
Styles APA, Harvard, Vancouver, ISO, etc.
2

Temenoff, Johnna S. « A Modular System to Examine Fibroblastic Differentiation of Mesenchymal Stem Cells Under Tensile Loading in Response to Changes in the Extracellular Environment ». Dans ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-53704.

Texte intégral
Résumé :
Hundreds of thousands of injuries to ligaments, tendons or the joint capsule occur in the U.S. each year, resulting in significant reduction of quality of life for many patients [1]. Existing reconstruction techniques for torn tendons/ligaments result in significant morbidity and cannot fully recapitulate the native joint biomechanics, leading to secondary degeneration over time, such as premature osteoarthritis. Thus, tissue-engineered alternatives to current grafts, potentially using stem cells in combination with an appropriate scaffold, are greatly needed. In response, our laboratory is investigating a novel hydrogel system and a custom tensile bioreactor as an in-vitro model to study the formation of both fibrous (ligament) tissue and the ligament-bone interface. In these studies, we examine the effect of tensile loading and the degradability of the surrounding environment on cellular morphology and tendon/ligament extracellular matrix (ECM) production by mesenchymal stem cells (MSCs). In particular, the response of MSCs embedded within hydrogels with varying degrees of susceptibility to degradation by collagenase is explored. In addition, proof-of-principle experiments are presented to extend this system to examine the effect of co-culture of multiple cell types on differentiation of MSCs in a milieu that mimics the bone-ligament insertion.
Styles APA, Harvard, Vancouver, ISO, etc.

Rapports d'organisations sur le sujet "Cell culture techniques – laboratory manuals"

1

Corscadden, Louise, et Anjali Singh. Methods Of Cleaning And Sterilization. Maze Engineers, décembre 2022. http://dx.doi.org/10.55157/cs20221207.

Texte intégral
Résumé :
Microbiology, tissue culture, medical, equipment manufacturing labs, and many research labs and industries need strict sterile environments for their diverse operations. Experiments, specifically those involving cell lines or microorganisms need to be conducted in a controlled environment. Contamination not only voids experiments, but also wastes effort, time, and money and when involving patients, it poses serious health risks. It is essential to be well-versed in laboratory sterilization techniques.
Styles APA, Harvard, Vancouver, ISO, etc.
Vous pouvez également être intéressé par les bibliographies sur le sujet « Cell culture techniques – laboratory manuals » pour d’autres types de sources :
Articles de revues Livres
Nous offrons des réductions sur tous les plans premium pour les auteurs dont les œuvres sont incluses dans des sélections littéraires thématiques. Contactez-nous pour obtenir un code promo unique!

Vers la bibliographie