anti mouse cd206 antibody (Elabscience Biotechnology)
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Elabscience Biotechnology
anti mouse cd206 antibody
Anti Mouse Cd206 Antibody, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 59 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+mouse+cd206+antibody/PE+Anti-Mouse+CD206%2FMMR+Antibody/pmc13091142-309-8-11
Average 95 stars, based on 59 article reviews
Anti Mouse Cd206 Antibody, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 59 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+mouse+cd206+antibody/PE+Anti-Mouse+CD206%2FMMR+Antibody/pmc13091142-309-8-11
Average 95 stars, based on 59 article reviews
anti mouse cd206 antibody - by Bioz Stars,
2026-09
95/100 stars
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1) Product Images from "Injection site dictates the immune response to a biodegradable polymer and corresponding collagen regeneration"
Article Title: Injection site dictates the immune response to a biodegradable polymer and corresponding collagen regeneration
Journal: Bioactive Materials
doi: 10.1016/j.bioactmat.2026.04.004
Figure Legend Snippet: LA released from T-gel degradation induces macrophage M2 polarization and promotes fibroblast activation and collagen production. (A) Flow cytometry analysis of the association between T-gel degradation products and macrophage M2 polarization ( n = 3, data represent mean ± s.d.). ∗∗∗∗P < 0.0001. (B) RNA-seq analysis of M2 macrophage marker expression in tissues one week after ID and SC injection of T-gel. (C–D) Immunofluorescence analysis of CD206 (C) and FAPα (D) expression in tissues ( n = 3, data represent mean ± s.d.). ∗∗P < 0.01. (E) Schematic diagram of the co-culture system showing RAW264.7 macrophages pretreated with T-gel extract medium that were subsequently co-cultured with L929 fibroblasts. (F–G) Collagen expression in L929 cells from the co-culture system assessed by Western blot (F) and ELISA (G). “C” represents RAW264.7 pretreated with blank medium; “T” represents RAW264.7 pretreated with T-gel extract medium. n = 3, data represent mean ± s.d. ∗P < 0.05 and ∗∗P < 0.01. (H) ELISA analysis of TGFβ expression in RAW264.7 cells treated with T-gel extract medium ( n = 3, data represent mean ± s.d.). ∗∗P < 0.01. (I) Schematic representation of LA, released during T-gel degradation, programming macrophages toward an M2 phenotype and subsequently promoting fibroblast activation and collagen secretion.
Techniques Used: Activation Assay, Flow Cytometry, RNA Sequencing, Marker, Expressing, Injection, Immunofluorescence, Co-Culture Assay, Cell Culture, Western Blot, Enzyme-linked Immunosorbent Assay
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