Yazarlar Miltenyi Biotec GmbH, Almanya çalışanları.

Steril koşullar altında çalışmak için, bir laminer akış kaputun içindeki tüm adımları gerçekleştirmek için tavsiye edilir. 1. Malzemeler <ol><li> HEPES tamponu: 10 mM HEPES-NaOH pH 7.4, 150 mM NaCl, 5 mM KCI, 1 mM MgCl 2, 1.8 mM CaCl 2) </li><li> Kollajenaz D çözüm: kollajenaz D: 100 mg / ml (kollajenaz D&gt; 0.15 U / mg) Hepes, tampon </li><li> DNaz I çözüm: 20.000 U / ml DNaz I </li><li> PBS pH 7,2 </li><li> PEB tampon: 20 kısım 1 kısım BSA Stok Çözüm Çözüm Durulama autoMACS </li><li> Doku: 6 / 7 hafta eski komşu organlara yetişkin erkek BALB / C fare, ikinci elde edilen akciğer. </li><li> İsteğe Bağlı: CD11c mikro, MACS MS Sütunlar fare akciğer tek hücre süspansiyonu dendritik hücrelerin izolasyonu için MACS Ayırıcı </li></ol> 2. Akciğer dokusu Dissociating <ol><li> Eritrositler kaldırmak için PBS içeren bir Petri kabındaki doku durulayın. </li><li> 4.9 mL HEPES tamponu içeren bir gentleMACS C Tüp maksimum 450 mg akciğer dokusunda bir aktarın. </li><li> 2 mg / ml kollajenaz D. nihai konsantrasyonu 100 mcL kollajenaz Ge çözüm </li><li> 150 mg doku (40 U / ml DNaz I final konsantrasyon) veya 150-450 mg akciğer dokusunda için 20 mcL DNaz I (80 U / ml DNaz I final konsantrasyon) için 10 mcL DNaz I çözüm ekleyin. </li><li> Sıkıca C Tüp yakın ve gentleMACS Dissociator üzerine ekleyin. Sonra programı çalıştırın &quot;m_lung_01&quot;. </li><li> 37 ° 30 dakika ° C&#39;de otomatik rotasyon veya elle her 5 dakikada bir dönüm. </li><li> GentleMACS Dissociator örnek dönün ve &quot;m_lung_02&quot; programı çalıştırın. </li></ol> 3. Süzme <ol><li> 70 mikron mesh hücre süzgecinden kap değiştirerek filtre hücreleri toplamak için 50 ml tüp hazırlayın. </li><li> Sonra ikinci gentleMACS Programı tüp örnek malzeme dağıtımı bağlı olarak, biter, tüpün alt kısmında örnek malzeme toplamak için kısaca tüp santrifüj olabilir. </li><li> Uygun bir 1000 ul pipet kullanarak C Boru septum kapalı kap aracılığıyla hücreleri hücre süzgeç çıkarın ve bunları uygulamak. </li><li> RT 5 ml HEPES tamponu ile hücre süzgeç yıkayın. </li><li> 10 dakika 300xg 50 ml tüp hücreleri bir pelet Santrifüj. </li><li> Süpernatantı aspire ve PEB tampon istenen hacmi hücre pelletini tekrar süspansiyon haline getirin. </li></ol> Bölüm 4: Temsilcilik Sonuçları: <img src="/files/ftp_upload/1266/1266fig1.jpg" alt="Şekil 1" /> Şekil 1: Akciğer disosiasyon gentleMACS ™ Dissociator% 92 canlı hücreler ile sonuçlandı. Ölü hücreler floresan propidium iyodür (PI (); PI boyama sol nokta arsa sağ nokta arsa) ile boyandı. <img src="/files/ftp_upload/1266/1266fig2.jpg" alt="Şekil 2" /> Şekil 2 fare akciğer dokusunun canlı lökosit ve endotel hücreleri yüksek oranda gentleMACS Dissociator sonuçlarını kullanarak Ayrılma. CD45-PE ve CD146-FITC veya CD31-FITC kökenli tek hücre süspansiyonları ile boyandı ve flow sitometri ile analiz edildi. <img src="/files/ftp_upload/1266/1266figure2c.png" alt="Şekil 2c" /> Şekil 3 fare akciğer dokusundan elde edilen tek hücre süspansiyonu CD11c-FITC ve Anti-mPDCA-1-APC fare CD11c düşük m-PUKÖ-1 + plazmasitoid DC&#39;ler yanı sıra CD11c yüksek hücreleri algılamak için boyandı . <img src="/files/ftp_upload/1266/1266fig4.jpg" alt="Şekil 4" /> Şekil 4 CD11c mikro, MiniMACS Ayırıcı ve iki MS Sütunlar kullanarak dendritik hücrelerin zenginleştirilmesi.

<ol>
	<li>Swanson, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Flt3-Ligand,+IL-4,+GM-CSF,+and+Adherence-Mediated+Isolation+of+Murine+Lung+Dendritic+Cells:+Assessment+of+Isolation+Technique+on+Phenotype+and+Function.">Flt3-Ligand, IL-4, GM-CSF, and Adherence-Mediated Isolation of Murine Lung Dendritic Cells: Assessment of Isolation Technique on Phenotype and Function.</a> J. Immunol. 173, 4875-4881 (2004).</li><li>Vermaelen, K., Pauwels, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Accurate+and+simple+discrimination+of+mouse+pulmonary+dendritic+cell+and+macrophage+populations+by+flow+cytometry:+Methodology+and+new+insights.">Accurate and simple discrimination of mouse pulmonary dendritic cell and macrophage populations by flow cytometry: Methodology and new insights.</a> Cytometry Part A. 61A, 170-177 (2004).</li></ol>

The authors are employees of Miltenyi Biotec GmbH who make the instrument used in this article.

Bu video, fare akciğer dokusunun ayrışma için yeni bir yöntem tanıtmak. Biz akciğer dokusunun mekanik ve enzimatik tedavi bir arada yaşayabilir lökosit ve endotel hücreleri yüksek oranda vermiştir olduğunu göstermektedir. Özellikle, doku mekanik parçalanması gentleMACS Dissociator tarafından elde edildi. Stator sistemi, yumuşak bir şekilde ayrışmaktadır doku gentleMACS C Tüpler bir rotor. Bu prosedür, cihazın program ayarları tarafından kontrol edilir. Ayarları, yüksek verim ve hücre canl?...

<table><tbody><tr><td>C Tubes</td><td>Miltenyi Biotec</td><td>Order no. 130-093-237</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_709_765_gentleMACS_C_Tubes.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_709_765_gentleMACS_C_Tubes.aspx&lt;/a&gt;</td></tr><tr><td>gentleMACS&amp;#8482; Starting Kit</td><td>Miltenyi Biotec</td><td>Order no. 130-093-235</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_709_763_gentleMACS_Dissociator.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_709_763_gentleMACS_Dissociator.aspx&lt;/a&gt;</td></tr><tr><td>MACSmix&amp;#8482; Tube Rotator</td><td>Miltenyi Biotec</td><td>Order no. 130-090-753</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_34_251_MACSmix_Tube_Rotator.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_34_251_MACSmix_Tube_Rotator.aspx&lt;/a&gt;</td></tr><tr><td>autoMACS&amp;#8482; Rinsing Solution</td><td>Miltenyi Biotec</td><td>Order no. 130-091-222</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_134_155_autoMACS_Rinsing_Solution.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_134_155_autoMACS_Rinsing_Solution.aspx&lt;/a&gt;</td></tr><tr><td>MACS&amp;#174; BSA Stock Solution</td><td>Miltenyi Biotec</td><td>Order no. 130-091-376</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_33_295_MACS_BSA_Stock_Solution.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_33_295_MACS_BSA_Stock_Solution.aspx&lt;/a&gt;</td></tr><tr><td>CD11c MicroBeads</td><td>Miltenyi Biotec</td><td>Order No. 130-052-001</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_93_132_CD11c_MicroBeads.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_93_132_CD11c_MicroBeads.aspx&lt;/a&gt;</td></tr><tr><td>CD11c-FITC, CD11c-PE</td><td>Miltenyi Biotec</td><td>Order no. 130-092-026130-091-830</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_599_329_CD11c.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_599_329_CD11c.aspx&lt;/a&gt;</td></tr><tr><td>Anti-mPDCA-1-APC</td><td>Miltenyi Biotec</td><td>Order no. 130-091-963</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_599_325_Anti_mPDCA_1.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_599_325_Anti_mPDCA_1.aspx&lt;/a&gt;</td></tr><tr><td>CD146-FITC</td><td>Miltenyi Biotec</td><td>Order no. 130-092-026</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_599_417_CD146_LSEC_.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_599_417_CD146_LSEC_.aspx&lt;/a&gt;</td></tr><tr><td>CD45-PE</td><td>Miltenyi Biotec</td><td>Order no. 130-091-610</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_599_331_CD45.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_599_331_CD45.aspx&lt;/a&gt;</td></tr><tr><td>Propidium Iodide Solution</td><td>Miltenyi Biotec</td><td>Order no. 130-093-233</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_337_744_Propidium_Iodide_Solution.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_337_744_Propidium_Iodide_Solution.aspx&lt;/a&gt;</td></tr><tr><td>Art 1000 Reach Pipet Tips</td><td>Molecular BioProducts</td><td>Order no. 2079</td><td>&lt;a href=&quot;http://www.mbpinc.com/ASP/products.aspx?query_TipID=61&quot;&gt;http://www.mbpinc.com/ASP/products.aspx?query_TipID=61&lt;/a&gt;&lt;br/&gt;&lt;a href=&quot;http://www.mbpinc.com/html/products/art/display.html&quot;&gt;http://www.mbpinc.com/html/products/art/display.html&lt;/a&gt;</td></tr></tbody></table>

standardized preparation of single-cell suspensions from mouse lung tissue using the gentlemacs dissociator

Dokuların tek hücre süspansiyonları hazırlık hücre araştırmalarında birçok deneyler için önemli bir ön koşuldur. Bütün organlar dissociating süreci, tekrarlanabilir bir şekilde yüksek bir sayıda canlı hücreleri elde etmek için belirli parametreler gerektirir. GentleMACS Dissociator basit, pratik bir protokol ile bu görevi en iyi hale getirir. Cihaz fare akciğerler dahil olmak üzere çeşitli doku tipleri, verimli ama nazik ayrılma için optimize edilmiş, önceden programlanmış ayarları içerir. Bu yayında farelerden elde edilen akciğer dokusunda gentleMACS Dissociator kullanımı gösterilmiştir.

Watch this Scientific Journal Video about Standardized Preparation of Single-Cell Suspensions from Mouse Lung Tissue using the gentleMACS Dissociator at JoVE.com

Standardized Preparation of Single-Cell Suspensions from Mouse Lung Tissue using the gentleMACS Dissociator

Belirli doku tiplerinin hücreleri Dissociating doku ajitasyon için belirli parametreler uygulanabilir kültürlenebilen hücrelerinin yüksek ses elde etmek için gereklidir. Miltenyi gentleMACS dissociator basit, pratik bir protokol ile bu görevi en iyi hale getirir. Bu yayında akciğer dokusunda bu cihazların kullanımı açıklanmıştır.

Standardize Hazırlık gentleMACS Dissociator kullanarak Fare Akciğer Doku Tek Hücre Cezalar

The preparation of single-cell suspensions from tissues is an important prerequisite for many experiments in cellular research. The process of ...

standardized-preparation-single-cell-suspensions-from-mouse-lung

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34.5K Görüntüleme.  Miltenyi Biotec,GmbH.  中文 日本語 

Video: Standardized Preparation of Single-Cell Suspensions from Mouse Lung Tissue using the gentleMACS Dissociator

Isolation of Mouse Lung Dendritic Cells

Lung dendritic cells (DC) play a fundamental role in sensing invading pathogens 1,2 as well as in the control of tolerogenic responses 3 in the respiratory tract. At least three main subsets of lung dendritic cells have been described in mice: conventional DC (cDC) 4, plasmacytoid DC (pDC) 5 and the IFN-producing killer DC (IKDC) 6,7. The cDC subset is the most prominent DC subset in the lung 8. 
The common marker known to identify DC subsets is CD11c, a type I transmembrane integrin (&beta;2) that is also expressed on monocytes, macrophages, neutrophils and some B cells 9. In some tissues, using CD11c as a marker to identify mouse DC is valid, as in spleen, where most CD11c+ cells represent the cDC subset which expresses high levels of the major histocompatibility complex class II (MHC-II). However, the lung is a more heterogeneous tissue where beside DC subsets, there is a high percentage of a distinct cell population that expresses high levels of CD11c bout low levels of MHC-II. Based on its characterization and mostly on its expression of F4&#47;80, an splenic macrophage marker, the CD11chiMHC-IIlo lung cell population has been identified as pulmonary macrophages 10 and more recently, as a potential DC precursor 11. 
In contrast to mouse pDC, the study of the specific role of cDC in the pulmonary immune response has been limited due to the lack of a specific marker that could help in the isolation of these cells. Therefore, in this work, we describe a procedure to isolate highly purified mouse lung cDC. The isolation of pulmonary DC subsets represents a very useful tool to gain insights into the function of these cells in response to respiratory pathogens as well as environmental factors that can trigger the host immune response in the lung.

A highly purified preparation of mouse lung dendritic cells is described. Specific emphasis is given to the isolation of conventional dendritic cell subset.

Fare Akciğer Dendritik Hücrelerinin İzolasyonu

Lung dendritic cells (DC) play a fundamental role in sensing invading pathogens 1,2 as well as in the control of tolerogenic responses 3 in the ...

İmmünoloji ve Enfeksiyon

Preparation of Single-Cell Suspensions from Mouse Spleen with the gentleMACS Dissociator

Single-cell suspensions are a prerequisite for experiments in cell separation, cell analysis and cell culture.  To avoid tedious and often painful manual dissociations the gentleMACS Dissociator allows one to dissociate tissue very efficiently under controlled and reproducible conditions.  The gentleMACS Dissociator can optimally dissociate mouse spleen, combining timesaving and standardization with user-safety.

This video describes how to dissociate mouse spleens using the gentleMACS Dissociator, an automated bench-top device that can mechanically disrupt tissues using special tubes to produce viable cell suspensions. Following dissociation, spleens are filtered, centrifuged, and resuspended for further applications.

This video describes a simple, time-saving technique for automated tissue dissociation using the gentleMACS Dissociator to prepare single-cell suspensions of mouse splenocytes.

Fare Dalak gentleMACS Dissociator Tek Hücreli Cezalar hazırlanması

Single-cell suspensions are a prerequisite for experiments in cell separation, cell analysis and cell culture.  To avoid tedious and often painful manual ...

Biyoloji

Generation of Single-Cell Suspensions from Mouse Neural Tissue

Within the nervous system, hundreds of neuronal and glial cell types have been described. Each specific cell type in the brain or spinal cord has a repertoire of cell surface molecules, or molecular determinants, through which it can be identified and characterized. Currently, robust cell identification and separation technologies require single-cell preparations to be generated while simultaneously limiting cell death and destruction of characteristic surface protein. The gentleMACS Dissociator, when used in combination with trypsin or papain-based dissociation kits, can effectively and gently dissociate brain tissue while preserving antigen epitopes and limiting cell loss. Standardized preparation of single-cell suspensions is achieved using C Tubes and optimized, preset gentleMACS Programs. Once generated, single-cell suspensions can be treated with monoclonal conjugates like Anti-Prominin-1 MicroBeads, which identify neural progenitors, or purified further using Myelin Removal Beads.

Dissociating cells from specific tissue types requires specific parameters for tissue aggitation to obtain a high volume of viable, culturable cells. The Miltenyi gentleMACS Dissociator optimizes this task with a simple, practical protocol. In this publication the use of this apparatus on nerual tissue is explained.

Fare Sinir Doku Hücre Tek Cezalar Üretimi

Within the nervous system, hundreds of neuronal and glial cell types have been described. Each specific cell type in the brain or spinal cord has a ...

Isolation and In Vitro Culture of Murine and Human Alveolar Macrophages

Alveolar macrophages are terminally differentiated, lung-resident macrophages of prenatal origin. Alveolar macrophages are unique in their long life and their important role in lung development and function, as well as their lung-localized responses to infection and inflammation. To date, no unified method for identification, isolation, and handling of alveolar macrophages from humans and mice exists. Such a method is needed for studies on these important innate immune cells in various experimental settings. The method described here, which can be easily adopted by any laboratory, is a simplified approach to harvesting alveolar macrophages from bronchoalveolar lavage fluid or from lung tissue and maintaining them in vitro. Because alveolar macrophages primarily occur as adherent cells in the alveoli, the focus of this method is on dislodging them prior to harvest and identification. The lung is a highly vascularized organ, and various cell types of myeloid and lymphoid origin inhabit, interact, and are influenced by the lung microenvironment. By using the set of surface markers described here, researchers can easily and unambiguously distinguish alveolar macrophages from other leukocytes, and purify them for downstream applications. The culture method developed herein supports both human and mouse alveolar macrophages for in vitro growth, and is compatible with cellular and molecular studies.

Isolation and In Vitro Culture of Murine and Human Alveolar Macrophages

This communication describes methodologies for isolation and culture of alveolar macrophages from humans and murine models for experimental purposes.

Yalıtım ve fare ve insan alveoler makrofajlar Vitro kültürü

Alveolar macrophages are terminally differentiated, lung-resident macrophages of prenatal origin. Alveolar macrophages are unique in their long life and ...

Isolation &#38; Characterization of Hoechstlow CD45negative Mouse Lung Mesenchymal Stem Cells

Tissue resident mesenchymal stem cells (MSC) are important regulators of tissue repair or regeneration, fibrosis, inflammation, angiogenesis and tumor formation. Taken together these studies suggest that resident lung MSC play a role during pulmonary tissue homeostasis, injury and repair during diseases such as pulmonary fibrosis (PF) and arterial hypertension (PAH). Here we describe a technology to define a population of resident lung MSC. The definition of this population in vivo pulmonary tissue using a define set of markers facilitates the repeated isolation of a well-characterized stem cell population by flow cytometry and the study of a specific cell type and function.

Isolation & Characterization of Hoechstlow CD45negative Mouse Lung Mesenchymal Stem Cells

In this article we demonstrate the isolation of murine resident lung mesenchymal stem cells (lung MSC), their expansion, characterization and analysis of immunomodulatory properties.

Hoechst İzolasyonu ve Karakterizasyonu Düşük CD45 Negatif Fare Akciğer Mezenkimal Kök Hücre

Tissue resident mesenchymal stem cells (MSC) are important regulators of tissue repair or regeneration, fibrosis, inflammation, angiogenesis and tumor ...

Tek hücreli analiz için yarı otomatik mekanik-enzimatik doku ayrışması

Mechanical Dissociation of Tissues for Single Cell Analysis Using a Motorized Device

Being able to isolate and prepare single cells for the analysis of tissue samples has rapidly become crucial for new biomedical discoveries and research. Manual protocols for single-cell isolations are highly time-consuming and prone to user variability. Automated mechanical protocols are able to reduce processing time and sample variability but aren't easily accessible or cost-effective in lower-resourced research settings. The device described here was designed for semi-automated tissue dissociation using commercially available materials as a low-cost alternative for academic laboratories. Instructions to fabricate, assemble, and operate the device design have been provided. The dissociation protocol reliably produces single-cell suspensions with comparable cell yields and sample viability to manual preparations across multiple mouse tissues. The protocol provides the ability to process up to 12 tissue samples simultaneously per device, making studies requiring large sample sizes more manageable. The accompanying software also allows for customization of the device protocol to accommodate varying tissues and experimental constraints.

Yazar Spotlight: İlaç Dağıtımı ve İmmünoterapi için Nanopartikül Teknolojisindeki Gelişmeler

A general protocol for the combined enzymatic and semi-automated mechanical dissociation of tissues to generate single-cell suspensions for downstream analyses, such as flow cytometry, is provided. Instructions for the fabrication, assembly, and operation of the low-cost mechanical device developed for this protocol are included.

Motorlu bir cihaz kullanarak tek hücre analizi için dokuların mekanik ayrışması

Being able to isolate and prepare single cells for the analysis of tissue samples has rapidly become crucial for new biomedical discoveries and research. ...

Biyomühendislik

Fare Akciğerlerinde Antijene Özgü T Hücrelerinin İzolasyonu ve Karakterizasyonu

Identification of Rare Antigen-Specific T Cells from Mouse Lungs with Peptide:Major Histocompatibility Complex Tetramers

The identification and characterization of antigen-specific T cells during health and disease remains a key to improving our understanding of immune pathophysiology. The technical challenges of tracking antigen-specific T cell populations within the endogenous T cell repertoire have been greatly advanced by the development of peptide:MHC tetramer reagents. These fluorescently labeled soluble multimers of MHC class I or class II molecules complexed to antigenic peptide epitopes bind directly to T cells with corresponding T cell receptor (TCR) specificity and can, therefore, identify antigen-specific T cell populations in their native state without a requirement for a functional response induced by ex vivo stimulation. For exceedingly rare populations, tetramer-bound T cells can be magnetically enriched to increase the sensitivity and reliability of detection.
As the investigation of tissue-resident T cell immunity deepens, there is a pressing need to identify antigen-specific T cells that traffic to and reside in nonlymphoid tissues. In this protocol, we present a detailed set of instructions for the isolation and characterization of antigen-specific T cells present within mouse lungs. This involves the isolation of T cells from digested lung tissue followed by a general T cell magnetic enrichment step and tetramer staining for flow cytometry analysis and sorting. The steps highlighted in this protocol utilize common techniques and readily available reagents, making it accessible for nearly any researcher engaged in mouse T cell immunology, and are highly adaptable for a variety of downstream analyses of any low frequency antigen-specific T cell population residing within the lungs.

Yazar Spotlight: Tetramerler Kullanarak Fare Akciğerlerinde Antijene Özgü T Hücrelerini Tespit Etmek için Optimize Edilmiş Protokol

We provide a detailed protocol for isolating and identifying rare antigen-specific T cell populations in mouse lungs through magnetic bead-based T cell enrichment and peptide:major histocompatibility complex (MHC) tetramers.

Fare Akciğerlerinden Nadir Antijene Özgü T Hücrelerinin Peptit ile Tanımlanması: Majör Histouyumluluk Kompleksi Tetramerleri

The identification and characterization of antigen-specific T cells during health and disease remains a key to improving our understanding of immune ...

Standardize Hazırlık gentleMACS Dissociator kullanarak Fare Akciğer Doku Tek Hücre Cezalar

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Özet

Daha Fazla Video Keşfet

Bu videodaki bölümler

Fare Akciğer Dendritik Hücrelerinin İzolasyonu

Fare Dalak gentleMACS Dissociator Tek Hücreli Cezalar hazırlanması

Fare Sinir Doku Hücre Tek Cezalar Üretimi

Yalıtım ve fare ve insan alveoler makrofajlar Vitro kültürü

Hoechst İzolasyonu ve Karakterizasyonu^Düşük CD45^Negatif Fare Akciğer Mezenkimal Kök Hücre

Motorlu bir cihaz kullanarak tek hücre analizi için dokuların mekanik ayrışması

Motorlu bir cihaz kullanarak tek hücre analizi için dokuların mekanik ayrışması

Motorlu bir cihaz kullanarak tek hücre analizi için dokuların mekanik ayrışması

Fare Akciğerlerinden Nadir Antijene Özgü T Hücrelerinin Peptit ile Tanımlanması: Majör Histouyumluluk Kompleksi Tetramerleri

Fare Akciğerlerinden Nadir Antijene Özgü T Hücrelerinin Peptit ile Tanımlanması: Majör Histouyumluluk Kompleksi Tetramerleri