mouse antibody subtype igg1 (MBL Life science)
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Mouse Antibody Subtype Igg1, supplied by MBL Life science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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1) Product Images from "A global chromatin compaction pathway that represses germline gene expression during starvation"
Article Title: A global chromatin compaction pathway that represses germline gene expression during starvation
Journal: The Journal of Cell Biology
doi: 10.1083/jcb.202009197
Figure Legend Snippet: Widespread H3K9 methylation is observed as chromatin compaction starts in C. elegans PGCs. (A) C. elegans embryos at different embryonic stages were fixed and stained for P-granules (green), H3K9me3 (red), and DNA (blue). Representative whole-embryo images are shown. (B) Same as A except only Z2/Z3 (germ) or a neighboring somatic cell (soma) is shown. The developmental stage of the embryo from which the image was taken is indicated ( n = 20). See for a summary of signal intensities. Scale bar represents a length of 2 µm.
Techniques Used: Methylation, Staining
Figure Legend Snippet: A TOP-2/condensin II–dependent increase in heterochromatin marks coincides with chromatin compaction in Z2/Z3. (A) Wild-type starved L1s and starved L1s that were defective for methyltransferases (mutants for met-2 , set-25 , set-32, and F1s from animals treated with met-2/set-25 double RNAi) were fixed and stained for P-granules (white), H3K9me2 (green), H3K9me3 (red), and DNA (blue). ( n = 40). See for a summary of signal intensities. (B) L1s were either starved or fed for a varying amount of time. Samples were then fixed and stained for P-granules (white), H3K9me3 (red), H3K9me2 (green), and DNA (blue). Representative images are shown. ( n = 40). See for a summary of signal intensities. (C) Starved L1s, born from strain N2 treated with either control RNAi or capg-2 RNAi, were fixed and stained for P-granules (white), H3K9me2 (green), H3K9me3 (red), and DNA (blue). Representative images are shown ( n = 40). See for a summary of signal intensities. (D) Starved L1s, born from strain N2 treated with either control or top-2 RNAi, were fixed and stained for H3K9me3 (red) and DNA (blue). Representative images are shown ( n = 40). See for a summary of signal intensities. (E) Worms that express HPL-2::mKate were optionally treated with control and capg-2 RNAi. Live embryos were extracted and were imaged for HPL-2 signal. The white star identifies Z2/Z3. Representative images are shown ( n = 20). (F) Quantification of HPL-2::mKate signal from the images taken in E. Error bars represent one standard deviation. Scale bar represents a length of 2 µm.
Techniques Used: Staining, Control, Standard Deviation
Figure Legend Snippet: Both H3K9 methyltransferases, MET-2 and SET-25, are needed for chromatin compaction in starved L1s. New and starved L1s born from strain WMM1 treated with either control RNAi, met-2 RNAi, or set-25 RNAi or met-2/set-25 double RNAi were used. Z2/Z3 from the L1s were imaged for chromatin compaction. Representative images are shown. Compaction was also quantified and shown below images. Error bars represent one standard deviation ( n = 20). Scale bar represents a length of 2 µm.
Techniques Used: Control, Standard Deviation
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