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Servicebio Inc pas staining kit
Pas Staining Kit, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pas+staining+kit/kit+pas+staining/pm42174638-76-6-12
Average 86 stars, based on 1 article reviews
pas staining kit - by Bioz Stars, 2026-10
86/100 stars

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Related Articles

TUNEL Assay:

Article Title: Ya Han Jie ameliorates adjuvant-induced arthritis by inhibiting the NF-κB/NETosis/inflammation axis.
Article Snippet: The H&E staining kit and a safranin O-fast green staining kit were purchased from Beijing Solarbio Science & Technology Co., Ltd. (Beijing, CHN). .. A TUNEL staining kit and a PAS staining kit were purchased from Servicebio (Wuhan, CHN). .. A toluidine blue staining kit was purchased from Beijing Leagene Biotechnology Co., Ltd. (Beijing, CHN).

Staining:

Article Title: Ya Han Jie ameliorates adjuvant-induced arthritis by inhibiting the NF-κB/NETosis/inflammation axis.
Article Snippet: The H&E staining kit and a safranin O-fast green staining kit were purchased from Beijing Solarbio Science & Technology Co., Ltd. (Beijing, CHN). .. A TUNEL staining kit and a PAS staining kit were purchased from Servicebio (Wuhan, CHN). .. A toluidine blue staining kit was purchased from Beijing Leagene Biotechnology Co., Ltd. (Beijing, CHN).

Article Title: HSPA1A-BAG5 chaperone complex promotes spermatogenesis by driving ubiquitination-mediated degradation of ATF2.
Article Snippet: Background: Male infertility represents a major global health challenge.. Heat shock protein A1A (HSPA1A), a stress-inducible molecular chaperone, shows potential importance in spermatogenesis, though its precise mechanistic role remains undefined.. Methods: Analysis of human sperm transcriptome data (GSE6969) revealed HSPA1A expression in fertile versus infertile samples.

Article Title: Nuclear receptor Nr1d1 links sleep deprivation to intestinal homeostasis via microbiota-derived taurine
Article Snippet: Stained slides were imaged using a light microscope, and quantitative analysis was performed using imageJ analysis software. .. Periodic acid-Schiff (PAS) staining was performed using the PAS staining kit (G1008-20 mL, Servicebio, Wuhan, China). .. Quantitative Immunohistochemical Methods: In this study, the quantitative analysis of IHC staining results was standardized using ImageJ software (version 1.8.0.112).

Article Title: Prrx1 promotes mesangial cell proliferation and kidney fibrosis through YAP in diabetic nephropathy
Article Snippet: .. The PAS staining kit was sourced from ServiceBio (Wuhan, China). ..

Article Title: Nuclear receptor Nr1d1 links sleep deprivation to intestinal homeostasis via microbiota-derived taurine.
Article Snippet: Stained slides were imaged using a light microscope, and quantitative analysis was performed using imageJ analysis software. .. Periodic acid-Schiff (PAS) staining was performed using the PAS staining kit (G1008-20 mL, Servicebio, Wuhan, China). .. Quantitative Immunohistochemical Methods: In this study, the quantitative analysis of IHC staining results was standardized using ImageJ software (version 1.8.0.112).

Article Title: THBS1 inhibition alleviates inflammatory response by inhibiting TGF-β and NLRP3 inflammasome in experimental murine dry eye.
Article Snippet: become essential in our lives.. Many people are addicted to cell phones, computers and games, which leads to increased prevalence of dry eye year by year.. Currently, the treatment strategy for dry eye mainly consists of increasing tears and anti-inflammatory treatment [4].

Article Title: Enhancing the structural stability of P29-targeted monoclonal antibodies via β-hydroxybutyrylation modification improves their therapeutic performance in alveolar echinococcosis
Article Snippet: .. PAS staining was conducted strictly according to the manufacturer’s protocol of PAS staining kit (G1008, Servicebio, China). .. All stained tissue sections were photographed under an upright optical microscope (NIKON ECLIPSE E100, Japan).

Article Title: Single-cell transcriptomic analysis unveils dysregulated macrophage-podocyte crosstalk in membranous nephropathy.
Article Snippet: Background: Membranous nephropathy (MN) is an antibody-mediated glomerular disease, but the cellular networks driving injury remain poorly defined.. Methods: We integrated the cationic bovine serum albumin (cBSA)-induced mouse MN model with single-cell RNA sequencing (scRNA-seq) to profile renal cells.. Bioinformatic analyses included clustering, differential expression, pathway enrichment, and cell-cell communication inference (CellChat).



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V. parvula exacerbates colonic mucus barrier damage in DSS-induced colitis mice, while the MGQD ameliorates this V. parvula -exacerbated damage. (A,B) <t>AB-PAS</t> staining in mouse colon. (C) The IF staining of mouse colon for Muc2 (red) and DAPI (blue). Data are expressed as mean ± S.D. (n = 6). #P < 0.05, ##P < 0.01, ###P < 0.001 vs. the DSV group. *P < 0.05, **P < 0.01, ***P < 0.001 vs. the DSS group.
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LPD improves colonic pathology (A) Serum LPS levels ( n = 8). (B) Morphological research measures include the number of goblet cells in the gland ( n = 3). (C) Representative pictures of HE staining, Scale bars, 100 μm. (D) Representative images <t>of</t> <t>Ab-PAS</t> staining, Scale bars, 100 μm. Data are presented as mean ± SEM ( n = 3–8 rats per group). For histological analyses, multiple sections and fields were averaged within each animal prior to statistical analysis. Statistical significance was determined by one-way ANOVA followed by Tukey’s post hoc test. ∗∗∗ p < 0.001.
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LPD improves colonic pathology (A) Serum LPS levels ( n = 8). (B) Morphological research measures include the number of goblet cells in the gland ( n = 3). (C) Representative pictures of HE staining, Scale bars, 100 μm. (D) Representative images <t>of</t> <t>Ab-PAS</t> staining, Scale bars, 100 μm. Data are presented as mean ± SEM ( n = 3–8 rats per group). For histological analyses, multiple sections and fields were averaged within each animal prior to statistical analysis. Statistical significance was determined by one-way ANOVA followed by Tukey’s post hoc test. ∗∗∗ p < 0.001.
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LPD improves colonic pathology (A) Serum LPS levels ( n = 8). (B) Morphological research measures include the number of goblet cells in the gland ( n = 3). (C) Representative pictures of HE staining, Scale bars, 100 μm. (D) Representative images <t>of</t> <t>Ab-PAS</t> staining, Scale bars, 100 μm. Data are presented as mean ± SEM ( n = 3–8 rats per group). For histological analyses, multiple sections and fields were averaged within each animal prior to statistical analysis. Statistical significance was determined by one-way ANOVA followed by Tukey’s post hoc test. ∗∗∗ p < 0.001.
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Mucus production, barrier integrity and cell viability evaluation for GoC characterization (A) Mucus production in co-culture 9:1 and 7:3 with <t>Alcian</t> blue/Periodic Acid Schiff’s staining. (B) Barrier integrity with LY (20 μg/ml) for co-culture 9:1 and 7:3 day 2, 4, 6, 8; blank - empty chip (Data are represented as mean ± SD. Test: One-way ANOVA t test, p < 0.01 “∗∗”, p < 0.0001 “∗∗∗∗”, n = 4). (C) Barrier integrity with LY (20 μg/ml) for co-culture 9:1 and 7:3 day 2, 4, 6, 8 (Data are represented as mean ± SD. Test: Two-way ANOVA t test, p < 0.05 “∗”, non-significant “ns”, n = 4). (D) Cell viability with CCK-8 cell viability kit for co-culture 9:1, 7:3 and viability control for co-culture 7:3 (0.25% Triton X-100 added in CM in flow for 24 hours at 2 μL/min) (Data are represented as mean ± SD. Test: One-way ANOVA t test, non-significant “ns”, p < 0.0001 “∗∗∗∗”, n = 4). (E) Variance using barrier integrity test with LY (20 μg/ml) for co-culture 7:3 day 2, 4, 6, 8 (Data are represented as mean ± SD. Test: Two-way ANOVA t test, p < 0.05 “∗”, p < 0.0001 “∗∗∗∗”, non-significant “ns”, n = 12–3 independent chips). (F) Variance using cell viability test with CCK-8 cell viability kit for co-culture 7:3 on day 8 in three chips independently No1, No2, No3 (n = 4) and all of them combined No1 + No2 + No3 (n = 12) (Data are represented as mean ± SD. Test: One-way ANOVA t test, non-significant “ns”).
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Image Search Results


V. parvula exacerbates colonic mucus barrier damage in DSS-induced colitis mice, while the MGQD ameliorates this V. parvula -exacerbated damage. (A,B) AB-PAS staining in mouse colon. (C) The IF staining of mouse colon for Muc2 (red) and DAPI (blue). Data are expressed as mean ± S.D. (n = 6). #P < 0.05, ##P < 0.01, ###P < 0.001 vs. the DSV group. *P < 0.05, **P < 0.01, ***P < 0.001 vs. the DSS group.

Journal: Frontiers in Pharmacology

Article Title: Modified gegen qinlian decoction ameliorates Veillonella parvula -exacerbated ulcerative colitis via restoration of intestinal mucosal barrier function

doi: 10.3389/fphar.2026.1803816

Figure Lengend Snippet: V. parvula exacerbates colonic mucus barrier damage in DSS-induced colitis mice, while the MGQD ameliorates this V. parvula -exacerbated damage. (A,B) AB-PAS staining in mouse colon. (C) The IF staining of mouse colon for Muc2 (red) and DAPI (blue). Data are expressed as mean ± S.D. (n = 6). #P < 0.05, ##P < 0.01, ###P < 0.001 vs. the DSV group. *P < 0.05, **P < 0.01, ***P < 0.001 vs. the DSS group.

Article Snippet: Hematoxylin and eosin (H&E) and Alcian Blue/Periodic Acid-Schiff (AB/PAS) staining kits were provided by Servicebio (Wuhan, China, Batch number:G1049).

Techniques: Staining

V. parvula exacerbates colonic barrier damage in DSS-induced colitis pseudo-germ-free mice, while the MGQD ameliorates this V. parvula -exacerbated damage. (A) The AB-PAS staining in mouse colon. (B) The IF staining of mouse colon for Muc2 (red) and DAPI (blue). (C) The Western blot of mouse colon. The data are expressed as the means ± S.D. (n = 6). *P < 0.05, **P < 0.01, ***P < 0.001 vs. the VD group.

Journal: Frontiers in Pharmacology

Article Title: Modified gegen qinlian decoction ameliorates Veillonella parvula -exacerbated ulcerative colitis via restoration of intestinal mucosal barrier function

doi: 10.3389/fphar.2026.1803816

Figure Lengend Snippet: V. parvula exacerbates colonic barrier damage in DSS-induced colitis pseudo-germ-free mice, while the MGQD ameliorates this V. parvula -exacerbated damage. (A) The AB-PAS staining in mouse colon. (B) The IF staining of mouse colon for Muc2 (red) and DAPI (blue). (C) The Western blot of mouse colon. The data are expressed as the means ± S.D. (n = 6). *P < 0.05, **P < 0.01, ***P < 0.001 vs. the VD group.

Article Snippet: Hematoxylin and eosin (H&E) and Alcian Blue/Periodic Acid-Schiff (AB/PAS) staining kits were provided by Servicebio (Wuhan, China, Batch number:G1049).

Techniques: Staining, Western Blot

LPD improves colonic pathology (A) Serum LPS levels ( n = 8). (B) Morphological research measures include the number of goblet cells in the gland ( n = 3). (C) Representative pictures of HE staining, Scale bars, 100 μm. (D) Representative images of Ab-PAS staining, Scale bars, 100 μm. Data are presented as mean ± SEM ( n = 3–8 rats per group). For histological analyses, multiple sections and fields were averaged within each animal prior to statistical analysis. Statistical significance was determined by one-way ANOVA followed by Tukey’s post hoc test. ∗∗∗ p < 0.001.

Journal: iScience

Article Title: Parabacteroides distasonis ameliorates ovariectomy-induced bone loss by regulating the gut microbiota and Th17/Treg balance

doi: 10.1016/j.isci.2026.115345

Figure Lengend Snippet: LPD improves colonic pathology (A) Serum LPS levels ( n = 8). (B) Morphological research measures include the number of goblet cells in the gland ( n = 3). (C) Representative pictures of HE staining, Scale bars, 100 μm. (D) Representative images of Ab-PAS staining, Scale bars, 100 μm. Data are presented as mean ± SEM ( n = 3–8 rats per group). For histological analyses, multiple sections and fields were averaged within each animal prior to statistical analysis. Statistical significance was determined by one-way ANOVA followed by Tukey’s post hoc test. ∗∗∗ p < 0.001.

Article Snippet: Ab-PAS Stain Kit , Servicebio , Cat. No. G1049.

Techniques: Staining

Mucus production, barrier integrity and cell viability evaluation for GoC characterization (A) Mucus production in co-culture 9:1 and 7:3 with Alcian blue/Periodic Acid Schiff’s staining. (B) Barrier integrity with LY (20 μg/ml) for co-culture 9:1 and 7:3 day 2, 4, 6, 8; blank - empty chip (Data are represented as mean ± SD. Test: One-way ANOVA t test, p < 0.01 “∗∗”, p < 0.0001 “∗∗∗∗”, n = 4). (C) Barrier integrity with LY (20 μg/ml) for co-culture 9:1 and 7:3 day 2, 4, 6, 8 (Data are represented as mean ± SD. Test: Two-way ANOVA t test, p < 0.05 “∗”, non-significant “ns”, n = 4). (D) Cell viability with CCK-8 cell viability kit for co-culture 9:1, 7:3 and viability control for co-culture 7:3 (0.25% Triton X-100 added in CM in flow for 24 hours at 2 μL/min) (Data are represented as mean ± SD. Test: One-way ANOVA t test, non-significant “ns”, p < 0.0001 “∗∗∗∗”, n = 4). (E) Variance using barrier integrity test with LY (20 μg/ml) for co-culture 7:3 day 2, 4, 6, 8 (Data are represented as mean ± SD. Test: Two-way ANOVA t test, p < 0.05 “∗”, p < 0.0001 “∗∗∗∗”, non-significant “ns”, n = 12–3 independent chips). (F) Variance using cell viability test with CCK-8 cell viability kit for co-culture 7:3 on day 8 in three chips independently No1, No2, No3 (n = 4) and all of them combined No1 + No2 + No3 (n = 12) (Data are represented as mean ± SD. Test: One-way ANOVA t test, non-significant “ns”).

Journal: STAR Protocols

Article Title: Protocol for developing a mucus-producing gut-on-a-chip model from Caco-2 and HT29-MTX-E12 cells

doi: 10.1016/j.xpro.2025.104321

Figure Lengend Snippet: Mucus production, barrier integrity and cell viability evaluation for GoC characterization (A) Mucus production in co-culture 9:1 and 7:3 with Alcian blue/Periodic Acid Schiff’s staining. (B) Barrier integrity with LY (20 μg/ml) for co-culture 9:1 and 7:3 day 2, 4, 6, 8; blank - empty chip (Data are represented as mean ± SD. Test: One-way ANOVA t test, p < 0.01 “∗∗”, p < 0.0001 “∗∗∗∗”, n = 4). (C) Barrier integrity with LY (20 μg/ml) for co-culture 9:1 and 7:3 day 2, 4, 6, 8 (Data are represented as mean ± SD. Test: Two-way ANOVA t test, p < 0.05 “∗”, non-significant “ns”, n = 4). (D) Cell viability with CCK-8 cell viability kit for co-culture 9:1, 7:3 and viability control for co-culture 7:3 (0.25% Triton X-100 added in CM in flow for 24 hours at 2 μL/min) (Data are represented as mean ± SD. Test: One-way ANOVA t test, non-significant “ns”, p < 0.0001 “∗∗∗∗”, n = 4). (E) Variance using barrier integrity test with LY (20 μg/ml) for co-culture 7:3 day 2, 4, 6, 8 (Data are represented as mean ± SD. Test: Two-way ANOVA t test, p < 0.05 “∗”, p < 0.0001 “∗∗∗∗”, non-significant “ns”, n = 12–3 independent chips). (F) Variance using cell viability test with CCK-8 cell viability kit for co-culture 7:3 on day 8 in three chips independently No1, No2, No3 (n = 4) and all of them combined No1 + No2 + No3 (n = 12) (Data are represented as mean ± SD. Test: One-way ANOVA t test, non-significant “ns”).

Article Snippet: EprediaTM Alcian Blue/PAS Special Stain Kit , Fisher Scientific , 23-900-664.

Techniques: Co-Culture Assay, Staining, CCK-8 Assay, Control