Product References
A simple and scalable 3D printing methodology for generating aligned and extended human and murine skeletal muscle tissues.
Biomedical materials (Bristol, England)
Cakal SD,Radeke C,Alcala JF,Ellman DG,Butdayev S,Andersen DC,Calloe K,Lind JU
MA1-22863 was used in Immunocytochemistry, Immunohistochemistry - Free Floating, Immunohistochemistry (Paraffin) to find high-resolution patterning is not required, as even patterns with feature sizes of several hundred micrometers is sufficient.
Tue May 17 00:00:00 UTC 2022
Recapitulating human cardio-pulmonary co-development using simultaneous multilineage differentiation of pluripotent stem cells.
eLife
Ng WH,Johnston EK,Tan JJ,Bliley JM,Feinberg AW,Stolz DB,Sun M,Wijesekara P,Hawkins F,Kotton DN,Ren X
MA1-22863 was used in Immunocytochemistry to report a novel stepwise strategy for directing the simultaneous induction of both mesoderm-derived cardiac and endoderm-derived lung epithelial lineages within a single differentiation of human-induced pluripotent stem cells (hiPSCs) via temporal specific tuning of WNT and nodal signaling in the absence of exogenous growth factors.
Wed Jan 12 00:00:00 UTC 2022
Cardiac ultrastructure inspired matrix induces advanced metabolic and functional maturation of differentiated human cardiomyocytes.
Cell reports
Afzal J,Liu Y,Du W,Suhail Y,Zong P,Feng J,Ajeti V,Sayyad WA,Nikolaus J,Yankova M,Deymier AC,Yue L
MA1-22863 was used in Flow cytometry/Cell sorting to present a method to accelerate hiPSC-CM maturation on a substrate, cardiac mimetic matrix (CMM), mimicking adult human heart matrix ligand chemistry, rigidity, and submicron ultrastructure, which synergistically mature hiPSC-CMs rapidly within 30 days.
Tue Jul 26 00:00:00 UTC 2022
Pre-clinical dose-escalation studies establish a therapeutic range for U7snRNA-mediated DMD exon 2 skipping.
Molecular therapy. Methods & clinical development
Simmons TR,Vetter TA,Huang N,Vulin-Chaffiol A,Wein N,Flanigan KM
MA1-22863 was used in Western Blot to develop an adeno-associated virus (AAV)-based U7snRNA exon-skipping approach directed toward exon 2, duplications of which represent 10% of all DMD duplication mutations.
Fri Jun 11 00:00:00 UTC 2021
Large-scale spontaneous self-organization and maturation of skeletal muscle tissues on ultra-compliant gelatin hydrogel substrates.
Scientific reports
Jensen JH,Cakal SD,Li J,Pless CJ,Radeke C,Jepsen ML,Jensen TE,Dufva M,Lind JU
MA1-22863 was used in Immunocytochemistry-immunoflourescence to show that C2C12 myoblasts spontaneously organize into highly aligned myotube tissues on the mm to cm scale, when cultured on sufficiently soft yet fully isotropic gelatin hydrogel substrates.
Thu Aug 06 00:00:00 UTC 2020
Large-scale spontaneous self-organization and maturation of skeletal muscle tissues on ultra-compliant gelatin hydrogel substrates.
Scientific reports
Jensen JH,Cakal SD,Li J,Pless CJ,Radeke C,Jepsen ML,Jensen TE,Dufva M,Lind JU
MA1-22863 was used in Immunocytochemistry-immunoflourescence to show that C2C12 myoblasts spontaneously organize into highly aligned myotube tissues on the mm to cm scale, when cultured on sufficiently soft yet fully isotropic gelatin hydrogel substrates.
Thu Aug 06 00:00:00 UTC 2020
Human Cardiac Organoids for Modeling Genetic Cardiomyopathy.
Cells
Filippo Buono M,von Boehmer L,Strang J,Hoerstrup SP,Emmert MY,Nugraha B
MA1-22863 was used in Immunocytochemistry to demonstrate the generation of cardiac organoids using a triculture approach of human induced pluripotent stem-cell-derived cardiomyocytes (hiPS-CMs)- from healthy subjects and cardiomyopathy patients-human cardiac microvascular endothelial cells (HCMECs) and human cardiac fibroblasts (HCFs).
Mon Jul 20 00:00:00 UTC 2020
On-site fabrication of Bi-layered adhesive mesenchymal stromal cell-dressings for the treatment of heart failure.
Biomaterials
Kobayashi K,Ichihara Y,Sato N,Umeda N,Fields L,Fukumitsu M,Tago Y,Ito T,Kainuma S,Podaru M,Lewis-McDougall F,Yamahara K,Uppal R,Suzuki K
MA1-22863 was used in Immunohistochemistry to address the issue of poor donor cell engraftment following current mesenchymal stromal/stem cell delivery methods.
Mon Jul 01 00:00:00 UTC 2019
Screening identifies small molecules that enhance the maturation of human pluripotent stem cell-derived myotubes.
eLife
Selvaraj S,Mondragon-Gonzalez R,Xu B,Magli A,Kim H,Lainé J,Kiley J,Mckee H,Rinaldi F,Aho J,Tabti N,Shen W,Perlingeiro RC
MA1-22863 was used in Immunocytochemistry to investigate pluripotent stem cells differentiation into myotubes in skeletal muscle disease.
Mon Nov 11 00:00:00 UTC 2019
Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis.
Human molecular genetics
Yang C,Xu Y,Yu M,Lee D,Alharti S,Hellen N,Ahmad Shaik N,Banaganapalli B,Sheikh Ali Mohamoud H,Elango R,Przyborski S,Tenin G,Williams S,O'Sullivan J,Al-Radi OO,Atta J,Harding SE,Keavney B,Lako M,Armstrong L
Published figure using alpha Sarcomeric Actinin monoclonal antibody (Product # MA1-22863) in Immunocytochemistry
Tue Aug 15 00:00:00 UTC 2017
From the Cover: High-Throughput Imaging of Cardiac Microtissues for the Assessment of Cardiac Contraction during Drug Discovery.
Toxicological sciences : an official journal of the Society of Toxicology
Pointon A,Pilling J,Dorval T,Wang Y,Archer C,Pollard C
MA1-22863 was used in Immunocytochemistry, Immunohistochemistry - Free Floating, Immunohistochemistry (Paraffin) to report that cardiac microtissues provide a high-throughput experimental model that is both able to detect changes in cardiac contraction with a sensitivity and specificity of 80 and 91%, respectively, and provide insight into the direction of the inotropic response.
Wed Feb 01 00:00:00 UTC 2017
An internal promoter underlies the difference in disease severity between N- and C-terminal truncation mutations of Titin in zebrafish.
eLife
Zou J,Tran D,Baalbaki M,Tang LF,Poon A,Pelonero A,Titus EW,Yuan C,Shi C,Patchava S,Halper E,Garg J,Movsesyan I,Yin C,Wu R,Wilsbacher LD,Liu J,Hager RL,Coughlin SR,Jinek M,Pullinger CR,Kane JP,Hart DO,Kwok PY,Deo RC
MA1-22863 was used in immunohistochemistry to characterize zebrafish with Titin truncations
Fri Oct 16 00:00:00 UTC 2015
Evolutionarily conserved intercalated disc protein Tmem65 regulates cardiac conduction and connexin 43 function.
Nature communications
Sharma P,Abbasi C,Lazic S,Teng ACT,Wang D,Dubois N,Ignatchenko V,Wong V,Liu J,Araki T,Tiburcy M,Ackerley C,Zimmermann WH,Hamilton R,Sun Y,Liu PP,Keller G,Stagljar I,Scott IC,Kislinger T,Gramolini AO
MA1-22863 was used in immunocytochemistry to investigate the impact of Tmem65 on heart development
Fri Sep 25 00:00:00 UTC 2015
Cyclin A2 induces cardiac regeneration after myocardial infarction through cytokinesis of adult cardiomyocytes.
Science translational medicine
Shapiro SD,Ranjan AK,Kawase Y,Cheng RK,Kara RJ,Bhattacharya R,Guzman-Martinez G,Sanz J,Garcia MJ,Chaudhry HW
MA1-22863 was used in immunocytochemistry and immunohistochemistry to study the role of adult cardiomyocyte cytokinesis in the mechanism by which adenoviral delivery of cyclin A2 to infarcted porcine heart promotes regeneration
Wed Feb 19 00:00:00 UTC 2014
Dystrophin-deficient cardiomyocytes derived from human urine: new biologic reagents for drug discovery.
Stem cell research
Guan X,Mack DL,Moreno CM,Strande JL,Mathieu J,Shi Y,Markert CD,Wang Z,Liu G,Lawlor MW,Moorefield EC,Jones TN,Fugate JA,Furth ME,Murry CE,Ruohola-Baker H,Zhang Y,Santana LF,Childers MK
MA1-22863 was used in immunohistochemistry to study the generation of cardiomyocytes from human urine-derived stem cells obtained from a patient with Duchenne muscular dystrophy
Sat Mar 01 00:00:00 UTC 2014
Amniotic fluid stem cells morph into a cardiovascular lineage: analysis of a chemically induced cardiac and vascular commitment.
Drug design, development and therapy
Maioli M,Contini G,Santaniello S,Bandiera P,Pigliaru G,Sanna R,Rinaldi S,Delitala AP,Montella A,Bagella L,Ventura C
MA1-22863 was used in immunocytochemistry to study the ability of a mixture of hyaluronic, butyric and retinoic acids to promote the differentiation of amniotic stem cells towards a cardiovascular lineage
Mon May 05 00:00:00 UTC 2014