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Fine Science Tools micro-spring scissors
Micro Spring Scissors, supplied by Fine Science Tools, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/micro-spring+scissors/spring+microscissors/pmc12188182-253-24-26
Average 90 stars, based on 1 article reviews
micro-spring scissors - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

Cell Culture:

Article Title: Methodology for generating chorioallantoic membrane patient-derived xenograft (CAM-PDX) models of pleural mesothelioma and performing preclinical imaging for the translation of cancer studies and drug screening.
Article Snippet: This was achieved using tweezers, such as No.5 110 mm tweezers (Dumont, Switzerland), to hold the CAM taut and cutting around the PDX with micro-spring scissors (Fine Science Tools, Germany) ensuring 0.5-1.0 cm of CAM remained around the sample.

Article Title: Monitoring of cell therapy and assessment of cardiac function using magnetic resonance imaging in a mouse model of myocardial infarction.
Article Snippet: We have developed a mouse severe combined immunodeficient (SCID) model of myocardial infarction based on permanent coronary artery occlusion that allows long-term functional analysis of engrafted human embryonic stem cell-derived cardiomyocytes, genetically marked with green fluorescent protein (GFP), in the mouse heart.. We describe methods for delivery of dissociated cardiomyocytes to the left ventricle that minimize scar formation and visualization and validation of the identity of the engrafted cells using the GFP emission spectrum, and histological techniques compatible with GFP epifluorescence, for monitoring phenotypic changes in the grafts in vivo.. In addition, we describe how magnetic resonance imaging can be adapted for use in mice to monitor cardiac function non-invasively and repeatedly.

Microscopy:

Article Title: Methodology for generating chorioallantoic membrane patient-derived xenograft (CAM-PDX) models of pleural mesothelioma and performing preclinical imaging for the translation of cancer studies and drug screening.
Article Snippet: This was achieved using tweezers, such as No.5 110 mm tweezers (Dumont, Switzerland), to hold the CAM taut and cutting around the PDX with micro-spring scissors (Fine Science Tools, Germany) ensuring 0.5-1.0 cm of CAM remained around the sample.

Article Title: Monitoring of cell therapy and assessment of cardiac function using magnetic resonance imaging in a mouse model of myocardial infarction.
Article Snippet: We have developed a mouse severe combined immunodeficient (SCID) model of myocardial infarction based on permanent coronary artery occlusion that allows long-term functional analysis of engrafted human embryonic stem cell-derived cardiomyocytes, genetically marked with green fluorescent protein (GFP), in the mouse heart.. We describe methods for delivery of dissociated cardiomyocytes to the left ventricle that minimize scar formation and visualization and validation of the identity of the engrafted cells using the GFP emission spectrum, and histological techniques compatible with GFP epifluorescence, for monitoring phenotypic changes in the grafts in vivo.. In addition, we describe how magnetic resonance imaging can be adapted for use in mice to monitor cardiac function non-invasively and repeatedly.

Sterility:

Article Title: Methodology for generating chorioallantoic membrane patient-derived xenograft (CAM-PDX) models of pleural mesothelioma and performing preclinical imaging for the translation of cancer studies and drug screening.
Article Snippet: This was achieved using tweezers, such as No.5 110 mm tweezers (Dumont, Switzerland), to hold the CAM taut and cutting around the PDX with micro-spring scissors (Fine Science Tools, Germany) ensuring 0.5-1.0 cm of CAM remained around the sample.

Article Title: Monitoring of cell therapy and assessment of cardiac function using magnetic resonance imaging in a mouse model of myocardial infarction.
Article Snippet: We have developed a mouse severe combined immunodeficient (SCID) model of myocardial infarction based on permanent coronary artery occlusion that allows long-term functional analysis of engrafted human embryonic stem cell-derived cardiomyocytes, genetically marked with green fluorescent protein (GFP), in the mouse heart.. We describe methods for delivery of dissociated cardiomyocytes to the left ventricle that minimize scar formation and visualization and validation of the identity of the engrafted cells using the GFP emission spectrum, and histological techniques compatible with GFP epifluorescence, for monitoring phenotypic changes in the grafts in vivo.. In addition, we describe how magnetic resonance imaging can be adapted for use in mice to monitor cardiac function non-invasively and repeatedly.

Magnetic Resonance Imaging:

Article Title: Methodology for generating chorioallantoic membrane patient-derived xenograft (CAM-PDX) models of pleural mesothelioma and performing preclinical imaging for the translation of cancer studies and drug screening.
Article Snippet: This was achieved using tweezers, such as No.5 110 mm tweezers (Dumont, Switzerland), to hold the CAM taut and cutting around the PDX with micro-spring scissors (Fine Science Tools, Germany) ensuring 0.5-1.0 cm of CAM remained around the sample.

Article Title: Monitoring of cell therapy and assessment of cardiac function using magnetic resonance imaging in a mouse model of myocardial infarction.
Article Snippet: We have developed a mouse severe combined immunodeficient (SCID) model of myocardial infarction based on permanent coronary artery occlusion that allows long-term functional analysis of engrafted human embryonic stem cell-derived cardiomyocytes, genetically marked with green fluorescent protein (GFP), in the mouse heart.. We describe methods for delivery of dissociated cardiomyocytes to the left ventricle that minimize scar formation and visualization and validation of the identity of the engrafted cells using the GFP emission spectrum, and histological techniques compatible with GFP epifluorescence, for monitoring phenotypic changes in the grafts in vivo.. In addition, we describe how magnetic resonance imaging can be adapted for use in mice to monitor cardiac function non-invasively and repeatedly.

Laser-Scanning Microscopy:

Article Title: Methodology for generating chorioallantoic membrane patient-derived xenograft (CAM-PDX) models of pleural mesothelioma and performing preclinical imaging for the translation of cancer studies and drug screening.
Article Snippet: This was achieved using tweezers, such as No.5 110 mm tweezers (Dumont, Switzerland), to hold the CAM taut and cutting around the PDX with micro-spring scissors (Fine Science Tools, Germany) ensuring 0.5-1.0 cm of CAM remained around the sample.

Article Title: Monitoring of cell therapy and assessment of cardiac function using magnetic resonance imaging in a mouse model of myocardial infarction.
Article Snippet: We have developed a mouse severe combined immunodeficient (SCID) model of myocardial infarction based on permanent coronary artery occlusion that allows long-term functional analysis of engrafted human embryonic stem cell-derived cardiomyocytes, genetically marked with green fluorescent protein (GFP), in the mouse heart.. We describe methods for delivery of dissociated cardiomyocytes to the left ventricle that minimize scar formation and visualization and validation of the identity of the engrafted cells using the GFP emission spectrum, and histological techniques compatible with GFP epifluorescence, for monitoring phenotypic changes in the grafts in vivo.. In addition, we describe how magnetic resonance imaging can be adapted for use in mice to monitor cardiac function non-invasively and repeatedly.

Software:

Article Title: Methodology for generating chorioallantoic membrane patient-derived xenograft (CAM-PDX) models of pleural mesothelioma and performing preclinical imaging for the translation of cancer studies and drug screening.
Article Snippet: This was achieved using tweezers, such as No.5 110 mm tweezers (Dumont, Switzerland), to hold the CAM taut and cutting around the PDX with micro-spring scissors (Fine Science Tools, Germany) ensuring 0.5-1.0 cm of CAM remained around the sample.

Article Title: Monitoring of cell therapy and assessment of cardiac function using magnetic resonance imaging in a mouse model of myocardial infarction.
Article Snippet: We have developed a mouse severe combined immunodeficient (SCID) model of myocardial infarction based on permanent coronary artery occlusion that allows long-term functional analysis of engrafted human embryonic stem cell-derived cardiomyocytes, genetically marked with green fluorescent protein (GFP), in the mouse heart.. We describe methods for delivery of dissociated cardiomyocytes to the left ventricle that minimize scar formation and visualization and validation of the identity of the engrafted cells using the GFP emission spectrum, and histological techniques compatible with GFP epifluorescence, for monitoring phenotypic changes in the grafts in vivo.. In addition, we describe how magnetic resonance imaging can be adapted for use in mice to monitor cardiac function non-invasively and repeatedly.

Fluorescence:

Article Title: Methodology for generating chorioallantoic membrane patient-derived xenograft (CAM-PDX) models of pleural mesothelioma and performing preclinical imaging for the translation of cancer studies and drug screening.
Article Snippet: This was achieved using tweezers, such as No.5 110 mm tweezers (Dumont, Switzerland), to hold the CAM taut and cutting around the PDX with micro-spring scissors (Fine Science Tools, Germany) ensuring 0.5-1.0 cm of CAM remained around the sample.

Article Title: Monitoring of cell therapy and assessment of cardiac function using magnetic resonance imaging in a mouse model of myocardial infarction.
Article Snippet: We have developed a mouse severe combined immunodeficient (SCID) model of myocardial infarction based on permanent coronary artery occlusion that allows long-term functional analysis of engrafted human embryonic stem cell-derived cardiomyocytes, genetically marked with green fluorescent protein (GFP), in the mouse heart.. We describe methods for delivery of dissociated cardiomyocytes to the left ventricle that minimize scar formation and visualization and validation of the identity of the engrafted cells using the GFP emission spectrum, and histological techniques compatible with GFP epifluorescence, for monitoring phenotypic changes in the grafts in vivo.. In addition, we describe how magnetic resonance imaging can be adapted for use in mice to monitor cardiac function non-invasively and repeatedly.



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Image Search Results


Dissection of SMA under microscope after heart perfusion (A) Identify the original area of SMA under a dissecting microscope. (B) Clear the stemming area of SMA. (C) Return the gastrointestinal tract to the physiological position. (D) Turn up the stomach and pancreas to display SMA. (E and F) Lift the transverse colon up and clean up the contaminants to exhibit SMA. (G–J) Trace the branches of SMA along the main course. (K) Cut off the mesenteric capillary network and isolate SMA. (L) SMA cleaned in a Sylgard coated dissection dish with PBS. a. Abdominal aorta; b. Superior mesenteric artery (SMA); c. celiac trunk; d. Right renal artery; e Inferior pancreatico-duodenal artery; f. Branches from SMA supplying for part of colon; g. Right posterior adrenal artery; h. Portal vein system; i. Branches from SMA supplying for intestine. Scale bars denote 5 mm.

Journal: STAR Protocols

Article Title: Protocol for studying the superior mesenteric artery in mice using non-invasive micro-ultrasound imaging and anatomic dissection

doi: 10.1016/j.xpro.2025.103606

Figure Lengend Snippet: Dissection of SMA under microscope after heart perfusion (A) Identify the original area of SMA under a dissecting microscope. (B) Clear the stemming area of SMA. (C) Return the gastrointestinal tract to the physiological position. (D) Turn up the stomach and pancreas to display SMA. (E and F) Lift the transverse colon up and clean up the contaminants to exhibit SMA. (G–J) Trace the branches of SMA along the main course. (K) Cut off the mesenteric capillary network and isolate SMA. (L) SMA cleaned in a Sylgard coated dissection dish with PBS. a. Abdominal aorta; b. Superior mesenteric artery (SMA); c. celiac trunk; d. Right renal artery; e Inferior pancreatico-duodenal artery; f. Branches from SMA supplying for part of colon; g. Right posterior adrenal artery; h. Portal vein system; i. Branches from SMA supplying for intestine. Scale bars denote 5 mm.

Article Snippet: Roboz surgical micro dissecting spring scissors , Roboz , RS-5604.

Techniques: Dissection, Microscopy

Journal: STAR Protocols

Article Title: Protocol for studying the superior mesenteric artery in mice using non-invasive micro-ultrasound imaging and anatomic dissection

doi: 10.1016/j.xpro.2025.103606

Figure Lengend Snippet:

Article Snippet: Roboz surgical micro dissecting spring scissors , Roboz , RS-5604.

Techniques: Recombinant, Saline, Staining, Microscopy, Imaging, Cream, Ultrasound Gel, Ointment, Sterility, Dissection

Journal: STAR Protocols

Article Title: Protocol for quantifying murine cardiomyocyte cell division by single-cell suspension

doi: 10.1016/j.xpro.2024.103452

Figure Lengend Snippet:

Article Snippet: (Optional) Micro spring scissors (needed if doing neonatal ages) , Fine Science Tools , 14060-09.

Techniques: Recombinant, Software, Dissection, Microscopy, Labeling, Injection, Transferring

Table of Materials

Journal: Journal of visualized experiments : JoVE

Article Title: Optimizing Mouse Primary Lens Epithelial Cell Culture: A Comprehensive Guide to Trypsinization

doi: 10.3791/65912

Figure Lengend Snippet: Table of Materials

Article Snippet: Vannas micro-dissecting spring scissors , Roboz Surgical Instrument Co., Inc , RS-5608.

Techniques: Saline, Modification, Blocking Assay

Table of Materials

Journal: Journal of visualized experiments : JoVE

Article Title: Optimizing Mouse Primary Lens Epithelial Cell Culture: A Comprehensive Guide to Trypsinization

doi: 10.3791/65912

Figure Lengend Snippet: Table of Materials

Article Snippet: Vannas micro-dissecting spring scissors , Roboz Surgical Instrument Co., Inc , RS-5608.

Techniques: Saline, Modification, Blocking Assay