matrigel coated coverslips (Sarstedt)
86
Structured Review
Sarstedt
matrigel coated coverslips
Matrigel Coated Coverslips, supplied by Sarstedt, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/matrigel+coated+coverslips/coated+collagen+fibronectin+iv/pm41644016-213-24-26
Average 86 stars, based on 1 article reviews
Matrigel Coated Coverslips, supplied by Sarstedt, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/matrigel+coated+coverslips/coated+collagen+fibronectin+iv/pm41644016-213-24-26
Average 86 stars, based on 1 article reviews
matrigel coated coverslips - by Bioz Stars,
2026-09
86/100 stars
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Related Articles
Cell Culture:Article Title: MBNL2 dysfunction in outer radial glial cells is associated with disrupted corticogenesis in congenital myotonic dystrophy. Article Snippet: Cells were then plated in a Matrigelcoated 12-well culture plate (Sarstedt) in mTeSRTM Plus medium, supplemented with ROCK inhibitor 10 μM Y-27632 (Tocris) for 24 h. At ~60–80% confluency, cells were dissociated as single cells with Accutase (Sigma-Aldrich) and either seeded at a clonal dilution in mTeSRTM Plus Medium, supplemented with CloneRTM2 (STEMCELL Technologies) for 4 days or pelleted and flash-frozen in liquid nitrogen for further validation of CTG excision from the wild-type DMPK allele by PCR. .. Once colonies reached a sufficient size, each clone was manually picked and split, with one fraction cultured for expansion and the other plated on Fluorescence In Situ Hybridization:Article Title: MBNL2 dysfunction in outer radial glial cells is associated with disrupted corticogenesis in congenital myotonic dystrophy. Article Snippet: Cells were then plated in a Matrigelcoated 12-well culture plate (Sarstedt) in mTeSRTM Plus medium, supplemented with ROCK inhibitor 10 μM Y-27632 (Tocris) for 24 h. At ~60–80% confluency, cells were dissociated as single cells with Accutase (Sigma-Aldrich) and either seeded at a clonal dilution in mTeSRTM Plus Medium, supplemented with CloneRTM2 (STEMCELL Technologies) for 4 days or pelleted and flash-frozen in liquid nitrogen for further validation of CTG excision from the wild-type DMPK allele by PCR. .. Once colonies reached a sufficient size, each clone was manually picked and split, with one fraction cultured for expansion and the other plated on |