software controlled microscope stage h117n2x2 stage for axiovert 200 (BFI Optilas GmbH)
90
Structured Review
BFI Optilas GmbH
software controlled microscope stage h117n2x2 stage for axiovert 200
Software Controlled Microscope Stage H117n2x2 Stage For Axiovert 200, supplied by BFI Optilas GmbH, 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/microscope+controller+software/software+controlled+microscope+stage+h117n2x2+stage+for+axiovert+200/pm25953320-63-25-32
Average 90 stars, based on 1 article reviews
Software Controlled Microscope Stage H117n2x2 Stage For Axiovert 200, supplied by BFI Optilas GmbH, 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/microscope+controller+software/software+controlled+microscope+stage+h117n2x2+stage+for+axiovert+200/pm25953320-63-25-32
Average 90 stars, based on 1 article reviews
software controlled microscope stage h117n2x2 stage for axiovert 200 - by Bioz Stars,
2026-09
90/100 stars
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Software:Article Title: 50 years to diagnosis: Autosomal dominant tubular aggregate myopathy caused by a novel STIM1 mutation. Article Snippet: Tubular aggregates in human muscle biopsies have been reported to occur in a variety of acquired and hereditary neuromuscular conditions since 1964.. Recently mutations in the gene encoding the main calcium sensor in the sarcoplasmic reticulum, stromal interaction molecule 1 (STIM1), have been identified as a cause of autosomal dominant tubular aggregate myopathy.. We studied a German family with tubular aggregate myopathy and defined cellular consequences of altered STIM1 function. Microscopy:Article Title: 50 years to diagnosis: Autosomal dominant tubular aggregate myopathy caused by a novel STIM1 mutation. Article Snippet: Tubular aggregates in human muscle biopsies have been reported to occur in a variety of acquired and hereditary neuromuscular conditions since 1964.. Recently mutations in the gene encoding the main calcium sensor in the sarcoplasmic reticulum, stromal interaction molecule 1 (STIM1), have been identified as a cause of autosomal dominant tubular aggregate myopathy.. We studied a German family with tubular aggregate myopathy and defined cellular consequences of altered STIM1 function. |