rab27a (Cell Signaling Technology Inc)
Structured Review

Rab27a, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 100 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+rab27a/Rab27A+Rabbit+mAb/bio_rxiv__64898__2026__03__25__713920-166-31-33
Average 95 stars, based on 100 article reviews
Images
1) Product Images from "Extracellular Vesicles from Senescent Tumor Cells Are Necessary and Sufficient to Drive Paracrine Senescence"
Article Title: Extracellular Vesicles from Senescent Tumor Cells Are Necessary and Sufficient to Drive Paracrine Senescence
Journal: bioRxiv
doi: 10.64898/2026.03.25.713920
Figure Legend Snippet: (a) RT-qPCR analysis of RAB27A . GAPDH was used as housekeeping gene. (b) Western blot analysis of RAB27A. Vinculin was used as loading control. (c) NTA analysis of particles in CM. (d) Representative images of morphology and SA-β-Gal staining (scale, 100 μm; scale in zoomed area, 200 μm). (e) Cell counting. (f) Cell size measurement. (g) Quantification of SA-β-Gal positive cells using X-gal substrate. (h) Quantification of SA-β-Gal positive cells using C 12 FDG substrate. (i) RT-qPCR analysis of CDKN1A . GAPDH was used as housekeeping gene. Significance was calculated using one-way ANOVA showing the exact p-value. Less than 0.05 was considered statistically significant (a, c-i, n=3; b, n=1).
Techniques Used: Quantitative RT-PCR, Western Blot, Control, Staining, Cell Counting
Figure Legend Snippet: (a) Representative images of morphology and SA-β-GAL staining (scale, 100 μm; scale in zoomed area, 200 μm). (b) Quantification of SA-β-GAL positive cells using X-gal substrate. (c) Flow cytometry plots of cells treated with conditioned media derived from control (CM-Scr), senescent (CM-Scr-S), or GW4869-treated senescent (CM-Scr-S+GW4869) cells, all of them expressing control Scrambled shRNA, and from RAB27A shRNA knockdown senescent cells (CM-shRAB27A #313-S). Significance was calculated using one-way ANOVA. Exact p-values are shown. Less than 0.05 was considered statistically significant (n=3).
Techniques Used: Staining, Flow Cytometry, Derivative Assay, Control, Expressing, shRNA, Knockdown
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