mouse anti-human aβ (82e1, 10323, tecan, 1:100 for if, 1:500 for wb) (Tecan Systems)
Structured Review

Mouse Anti Human Aβ (82e1, 10323, Tecan, 1:100 For If, 1:500 For Wb), supplied by Tecan Systems, 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/mouse+anti%E2%80%93human+a%CE%B2+82e1/pmc11607342-322-0-5?v=Tecan+Systems
Average 90 stars, based on 1 article reviews
Images
1) Product Images from "Altered expression of Presenilin2 impacts endolysosomal homeostasis and synapse function in Alzheimer’s disease-relevant brain circuits"
Article Title: Altered expression of Presenilin2 impacts endolysosomal homeostasis and synapse function in Alzheimer’s disease-relevant brain circuits
Journal: Nature Communications
doi: 10.1038/s41467-024-54777-y
Figure Legend Snippet: a Coronal hippocampal slices of APPKI, APPxPSEN2KO and APPxFADPSEN2 stained for thioflavin, labelling dense core plaques over time. b Quantification of thioflavin + area normalized to brain area for hippocampus over time and analyzed using two-way ANOVA using a Dunnett’s correction for multiple testing comparing the different conditions to APPKI. c Dual immunolabelling of Aβ plaques in coronal cortex sections using a fibrillar (fAβ) and monomeric Aβ specific antibody (82e1). d , e Average size ( d ) and number ( e ) of thioflavin + plaques calculated from ( a , c ). Statistical analysis was through a one-way ANOVA with a Dunnett’s correction for multiple testing compared to APPKI ( f ). Immunolabelling of 3 month old coronal hippocampal slices of APPKI, APPxPSEN2KO and APPxFADPSEN2 for Aβ/APP-CTF (82e1), LAMP1, full length APP and thioflavin. g Quantification of LAMP1 + area as a percent of total hippocampus area. For ( g ) a two-way ANOVA analysis with Tukey’s correction for multiple testing compared to APPKI was used. Scale bars and p -values are indicated; number of mice (N) is shown inside the bar and the symbols represent the number of regions analyzed. All graphs are mean ± SEM.
Techniques Used: Staining
Figure Legend Snippet: a Representative images of DIV14 hippocampal neurons immunostained for full length APP, APPCTF/Aβ (82e1) and LAMP1. Arrowheads in zoomed insets highlight co-localization. b Western blot of DIV14 neuronal lysates showing increased APP-CTF levels. c Quantification of a for triple overlap between LAMP1 and APP/82e1 positive puncta. d Quantification of ratio APP: APP-CTF ratio of blots from ( b ). e Representative images of immunolabeling of early (EEA1) and recycling endosomes (VPS35), and LE/Lys (LAMP1). White arrowheads in zoomed insets show overlap between three compartments. f – h Quantification of total area of ( f ) LAMP1, ( g ) EEA1 and ( h ) VPS35 as percentage of total neuronal soma area. i Representative images of lysosomal Ca 2+ measured through feeding cells with dextran coupled Alexa488 and Ca 2+ sensitive Rhodamine-coupled dextran, and quantified in ( j ) as a Rhodamine/Alexa488 ratio. k LAMP1 surface labelling combined with Phalloidin staining, quantified in ( l ). m Schematic of the dual labelled mCherry-GFP-LC3: in autophagosomes both mCherry and GFP give yellow fluorescence; whereas in lysosomes, GFP is quenched resulting in red fluorescence. Created in BioRender. Vrancx, C. (2024) https://BioRender.com/j26q595 . n Representative images of DIV14 hippocampal neurons transfected with mCherry-GFP-LC3, quantified in ( o ) as total number of mCherry+ LC3 puncta normalized to APPKI neurons and in ( p ) as total number of mCherry + /GFP + LC3 puncta. Graphs ( c – f – g – h – j – l – o – p ) were statistically analyzed using one-way ANOVA with Tukey’s correction for multiple testing compared to APPKI. All graphs are represented as mean ± SEM, with triangles and circles representing the average per neuronal culture and individual cells, respectively. Scale bars are indicated in the figure.
Techniques Used: Western Blot, Immunolabeling, Staining, Fluorescence, Transfection
