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Santa Cruz Biotechnology asc
Asc, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 153 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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asc - by Bioz Stars, 2026-10
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Related Articles

Polyacrylamide Gel Electrophoresis:

Article Title: Effects of arsenic exposure on D-serine metabolism in the hippocampus of offspring mice at different developmental stages.
Article Snippet: The main purpose of this study was to verify the hypothesis that cognitive dysfunctions induced by arsenic exposure were related to the changes of d-serine metabolism in the hippocampus of offspring mice.. Mother mice and their offsprings were exposed to 0, 15, 30 or 60 mg/L sodium arsenite (NaAsO2) through drinking water from the first day of gestation until the end of lactation. d-serine levels in the hippocampus of mice of postnatal day (PND) 10, 20 and 40 were examined by highperformance liquid chromatography.. Expressions of serine racemase (SR), d-amino acid oxidase (DAAO), alanine–serine– cysteine transporter-1 (asc-1) and subunits of N-methyl-d-aspartate receptors (NMDARs) in the hippocampus of mice were measured by Western blot and Real-time RT-PCR.

Immunodepletion:

Article Title: Gastrin activates paracrine networks leading to induction of PAI-2 via MAZ and ASC-1
Article Snippet: .. For immunodepletion experiments, nuclear extracts were preincubated (20 min) on ice with antibodies to Sp1-4, AP-2, ASC-1, TFIID (Santa Cruz Biotechnology), ZBP-89 (gift from J. ..

Staining:

Article Title: Isolation and characterization of white and brown adipocytes in Kunming mice.
Article Snippet: .. The cells were stained with primary antibodies against CD44, CD29, HLA-DR, CD34 (BIOSS, CN), ASC-1 (sc-292032, Santa Cruz, CA, USA), Ucp1 (ab10983, Abcam, UK), α-tubulin (ab15246, Abcam), and GAPDH (ab9485, Abcam) overnight at 4°C. ..

Western Blot:

Article Title: The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular Dystrophy.
Article Snippet: LPS (Sigma-Aldrich) was reconstituted at a final concentration of 1 mg/mL in HBSS and stored at –20 °C, ATP (Sigma-Aldrich) was reconstituted at 100 mM (pH 7) in H2O with NaOH and stored at –20 °C, Benzoyl ATP (BzATP) (Sigma-Aldrich) was reconstituted at 10 mM in H2O and stored at –20 °C. .. The antibodies and dilutions used in the study include the following: mouse monoclonal antibody to Collagen type I (1:500 for Western Blot [WB]) and rat monoclonal antibody to Ly6C (1:500 for Immunohistochemistry [IHC]) from Abcam (Cambridge, UK); rat monoclonal antibody to CD45 (1:10 for IHC) from BD Pharmigen (San Jose, CA); mouse monoclonal antibody to ASC-1 (1:500 for WB) and rabbit polyclonal antibodies to glyceraldehyde phosphate dehydrogenase (GAPDH) (1:500 for WB) from Santa Cruz Biotechnology (Santa Cruz, CA); rabbit polyclonal to CD3 (1:20 for IHC); rabbit polyclonal antibodies to P2X7R (extracellular) and P2X4R (1:50 and 1:300 respectively; for IF) from Alomone Labs (Jerusalem, Israel); rabbit polyclonal antibody to M AN US CR IP T AC CE PT ED ACCEPTED MANUSCRIPT 7 transforming growth factor (TGF)-β (1:1000 for WB) from Cell Signaling Technology (Danvers, MA); mouse monoclonal antibody to CD39 (1:1000) from Abcam; mouse monoclonal antibody to Alpha-Sarcoglycan (α-SG) (1:100 for WB) from Novocastra (Newcastle upon Tyne, UK) ; mouse monoclonal antibody to Beta-Dystroglycan (β-DG) (1:50 for WB) from Novocastra (Newcastle upon Tyne, UK); mouse monoclonal Anti-Caveolin 3 (1:10000 for WB) from BD Bioscience; mouse monoclonal antibody to Myosin Heavy Chain (fast) (MyHC) (1:1000 for WB) from Novocastra; rabbit anti-mouse IgG horseradish peroxidase (HRP)-conjugated (1:700 for WB) antibodies from Dako (Glostrup, Denmark); donkey anti-rabbit IgG HRP-conjugated (1:5000 for WB) from GE Healthcare (Little Chalfont, UK); mouse monoclonal anti-rat Kappa & Lambda Light Chains horseradish peroxidase (HRP)-conjugated (1:100 for IHC) antibody from SigmaAldrich; rat monoclonal to FOXP3 (1:20 for IHC) (eBioscience), goat anti-mouse AlexaFluor 488 and donkey anti-rat AlexaFluor 594 (1:750 for IF) antibodies from Thermo Fisher Scientific (Waltham, MA). .. The EnVision Detection System Peroxidase/diaminobenzidine, rabbit and mouse, were from Dako Annexin A5-FITC /7-AAD Kit was purchased from Beckman Coulter (Marseille, France).

Immunohistochemistry:

Article Title: The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular Dystrophy.
Article Snippet: LPS (Sigma-Aldrich) was reconstituted at a final concentration of 1 mg/mL in HBSS and stored at –20 °C, ATP (Sigma-Aldrich) was reconstituted at 100 mM (pH 7) in H2O with NaOH and stored at –20 °C, Benzoyl ATP (BzATP) (Sigma-Aldrich) was reconstituted at 10 mM in H2O and stored at –20 °C. .. The antibodies and dilutions used in the study include the following: mouse monoclonal antibody to Collagen type I (1:500 for Western Blot [WB]) and rat monoclonal antibody to Ly6C (1:500 for Immunohistochemistry [IHC]) from Abcam (Cambridge, UK); rat monoclonal antibody to CD45 (1:10 for IHC) from BD Pharmigen (San Jose, CA); mouse monoclonal antibody to ASC-1 (1:500 for WB) and rabbit polyclonal antibodies to glyceraldehyde phosphate dehydrogenase (GAPDH) (1:500 for WB) from Santa Cruz Biotechnology (Santa Cruz, CA); rabbit polyclonal to CD3 (1:20 for IHC); rabbit polyclonal antibodies to P2X7R (extracellular) and P2X4R (1:50 and 1:300 respectively; for IF) from Alomone Labs (Jerusalem, Israel); rabbit polyclonal antibody to M AN US CR IP T AC CE PT ED ACCEPTED MANUSCRIPT 7 transforming growth factor (TGF)-β (1:1000 for WB) from Cell Signaling Technology (Danvers, MA); mouse monoclonal antibody to CD39 (1:1000) from Abcam; mouse monoclonal antibody to Alpha-Sarcoglycan (α-SG) (1:100 for WB) from Novocastra (Newcastle upon Tyne, UK) ; mouse monoclonal antibody to Beta-Dystroglycan (β-DG) (1:50 for WB) from Novocastra (Newcastle upon Tyne, UK); mouse monoclonal Anti-Caveolin 3 (1:10000 for WB) from BD Bioscience; mouse monoclonal antibody to Myosin Heavy Chain (fast) (MyHC) (1:1000 for WB) from Novocastra; rabbit anti-mouse IgG horseradish peroxidase (HRP)-conjugated (1:700 for WB) antibodies from Dako (Glostrup, Denmark); donkey anti-rabbit IgG HRP-conjugated (1:5000 for WB) from GE Healthcare (Little Chalfont, UK); mouse monoclonal anti-rat Kappa & Lambda Light Chains horseradish peroxidase (HRP)-conjugated (1:100 for IHC) antibody from SigmaAldrich; rat monoclonal to FOXP3 (1:20 for IHC) (eBioscience), goat anti-mouse AlexaFluor 488 and donkey anti-rat AlexaFluor 594 (1:750 for IF) antibodies from Thermo Fisher Scientific (Waltham, MA). .. The EnVision Detection System Peroxidase/diaminobenzidine, rabbit and mouse, were from Dako Annexin A5-FITC /7-AAD Kit was purchased from Beckman Coulter (Marseille, France).



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A) Experimental diagram. B) wnnUMAPs of <t>ASCs</t> colored by tissue (left) or subset (right). Data from HD matched fixed CITEseq. C) Percent subset of total ASCs by sample. Data from HD matched fixed CITEseq. D) Percent subisotype usage by sample. Data from HD matched fixed CITEseq. E) Experimental diagram. F) Representative region of interest from a bone marrow core colored by fluorescence signal (top) or subset labels of segmented cells (bottom). Data from HD BM spatial proteomics. G) <t>Percent</t> <t>ASC</t> subset of total cells by individual. Data from HD BM spatial proteomics. H) Computational diagram. I) Observed (black diamond) and randomly permuted (grey density) percent of ASCs found in homotypic niches (defined as all ASCs in a niche having identical subset identities), by individual. Empirical p-values calculated as the number of permutations with homotypic niche frequencies greater or equal to the observed homotypic niche frequency, divided by the number of permutations plus one. Data from HD BM spatial proteomics. J) Computational diagram. K) Scaled enrichment scores of cell types (x-axis) in ASC subset (y-axis) niches by individual (panel). Q-values<0.1 were colored white. Data from HD BM spatial proteomics. L) Representative images (panels) of ASC-rich regions colored by fluorescence signal (left) or cell type labels of segmented cells (right). Data from HD BM spatial proteomics.
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A) Experimental diagram. B) wnnUMAPs of <t>ASCs</t> colored by tissue (left) or subset (right). Data from HD matched fixed CITEseq. C) Percent subset of total ASCs by sample. Data from HD matched fixed CITEseq. D) Percent subisotype usage by sample. Data from HD matched fixed CITEseq. E) Experimental diagram. F) Representative region of interest from a bone marrow core colored by fluorescence signal (top) or subset labels of segmented cells (bottom). Data from HD BM spatial proteomics. G) <t>Percent</t> <t>ASC</t> subset of total cells by individual. Data from HD BM spatial proteomics. H) Computational diagram. I) Observed (black diamond) and randomly permuted (grey density) percent of ASCs found in homotypic niches (defined as all ASCs in a niche having identical subset identities), by individual. Empirical p-values calculated as the number of permutations with homotypic niche frequencies greater or equal to the observed homotypic niche frequency, divided by the number of permutations plus one. Data from HD BM spatial proteomics. J) Computational diagram. K) Scaled enrichment scores of cell types (x-axis) in ASC subset (y-axis) niches by individual (panel). Q-values<0.1 were colored white. Data from HD BM spatial proteomics. L) Representative images (panels) of ASC-rich regions colored by fluorescence signal (left) or cell type labels of segmented cells (right). Data from HD BM spatial proteomics.
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A) Experimental diagram. B) wnnUMAPs of <t>ASCs</t> colored by tissue (left) or subset (right). Data from HD matched fixed CITEseq. C) Percent subset of total ASCs by sample. Data from HD matched fixed CITEseq. D) Percent subisotype usage by sample. Data from HD matched fixed CITEseq. E) Experimental diagram. F) Representative region of interest from a bone marrow core colored by fluorescence signal (top) or subset labels of segmented cells (bottom). Data from HD BM spatial proteomics. G) <t>Percent</t> <t>ASC</t> subset of total cells by individual. Data from HD BM spatial proteomics. H) Computational diagram. I) Observed (black diamond) and randomly permuted (grey density) percent of ASCs found in homotypic niches (defined as all ASCs in a niche having identical subset identities), by individual. Empirical p-values calculated as the number of permutations with homotypic niche frequencies greater or equal to the observed homotypic niche frequency, divided by the number of permutations plus one. Data from HD BM spatial proteomics. J) Computational diagram. K) Scaled enrichment scores of cell types (x-axis) in ASC subset (y-axis) niches by individual (panel). Q-values<0.1 were colored white. Data from HD BM spatial proteomics. L) Representative images (panels) of ASC-rich regions colored by fluorescence signal (left) or cell type labels of segmented cells (right). Data from HD BM spatial proteomics.
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A) Experimental diagram. B) wnnUMAPs of <t>ASCs</t> colored by tissue (left) or subset (right). Data from HD matched fixed CITEseq. C) Percent subset of total ASCs by sample. Data from HD matched fixed CITEseq. D) Percent subisotype usage by sample. Data from HD matched fixed CITEseq. E) Experimental diagram. F) Representative region of interest from a bone marrow core colored by fluorescence signal (top) or subset labels of segmented cells (bottom). Data from HD BM spatial proteomics. G) <t>Percent</t> <t>ASC</t> subset of total cells by individual. Data from HD BM spatial proteomics. H) Computational diagram. I) Observed (black diamond) and randomly permuted (grey density) percent of ASCs found in homotypic niches (defined as all ASCs in a niche having identical subset identities), by individual. Empirical p-values calculated as the number of permutations with homotypic niche frequencies greater or equal to the observed homotypic niche frequency, divided by the number of permutations plus one. Data from HD BM spatial proteomics. J) Computational diagram. K) Scaled enrichment scores of cell types (x-axis) in ASC subset (y-axis) niches by individual (panel). Q-values<0.1 were colored white. Data from HD BM spatial proteomics. L) Representative images (panels) of ASC-rich regions colored by fluorescence signal (left) or cell type labels of segmented cells (right). Data from HD BM spatial proteomics.
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A) Experimental diagram. B) wnnUMAPs of <t>ASCs</t> colored by tissue (left) or subset (right). Data from HD matched fixed CITEseq. C) Percent subset of total ASCs by sample. Data from HD matched fixed CITEseq. D) Percent subisotype usage by sample. Data from HD matched fixed CITEseq. E) Experimental diagram. F) Representative region of interest from a bone marrow core colored by fluorescence signal (top) or subset labels of segmented cells (bottom). Data from HD BM spatial proteomics. G) <t>Percent</t> <t>ASC</t> subset of total cells by individual. Data from HD BM spatial proteomics. H) Computational diagram. I) Observed (black diamond) and randomly permuted (grey density) percent of ASCs found in homotypic niches (defined as all ASCs in a niche having identical subset identities), by individual. Empirical p-values calculated as the number of permutations with homotypic niche frequencies greater or equal to the observed homotypic niche frequency, divided by the number of permutations plus one. Data from HD BM spatial proteomics. J) Computational diagram. K) Scaled enrichment scores of cell types (x-axis) in ASC subset (y-axis) niches by individual (panel). Q-values<0.1 were colored white. Data from HD BM spatial proteomics. L) Representative images (panels) of ASC-rich regions colored by fluorescence signal (left) or cell type labels of segmented cells (right). Data from HD BM spatial proteomics.
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A) Experimental diagram. B) wnnUMAPs of <t>ASCs</t> colored by tissue (left) or subset (right). Data from HD matched fixed CITEseq. C) Percent subset of total ASCs by sample. Data from HD matched fixed CITEseq. D) Percent subisotype usage by sample. Data from HD matched fixed CITEseq. E) Experimental diagram. F) Representative region of interest from a bone marrow core colored by fluorescence signal (top) or subset labels of segmented cells (bottom). Data from HD BM spatial proteomics. G) <t>Percent</t> <t>ASC</t> subset of total cells by individual. Data from HD BM spatial proteomics. H) Computational diagram. I) Observed (black diamond) and randomly permuted (grey density) percent of ASCs found in homotypic niches (defined as all ASCs in a niche having identical subset identities), by individual. Empirical p-values calculated as the number of permutations with homotypic niche frequencies greater or equal to the observed homotypic niche frequency, divided by the number of permutations plus one. Data from HD BM spatial proteomics. J) Computational diagram. K) Scaled enrichment scores of cell types (x-axis) in ASC subset (y-axis) niches by individual (panel). Q-values<0.1 were colored white. Data from HD BM spatial proteomics. L) Representative images (panels) of ASC-rich regions colored by fluorescence signal (left) or cell type labels of segmented cells (right). Data from HD BM spatial proteomics.
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Image Search Results


A) Experimental diagram. B) wnnUMAPs of ASCs colored by tissue (left) or subset (right). Data from HD matched fixed CITEseq. C) Percent subset of total ASCs by sample. Data from HD matched fixed CITEseq. D) Percent subisotype usage by sample. Data from HD matched fixed CITEseq. E) Experimental diagram. F) Representative region of interest from a bone marrow core colored by fluorescence signal (top) or subset labels of segmented cells (bottom). Data from HD BM spatial proteomics. G) Percent ASC subset of total cells by individual. Data from HD BM spatial proteomics. H) Computational diagram. I) Observed (black diamond) and randomly permuted (grey density) percent of ASCs found in homotypic niches (defined as all ASCs in a niche having identical subset identities), by individual. Empirical p-values calculated as the number of permutations with homotypic niche frequencies greater or equal to the observed homotypic niche frequency, divided by the number of permutations plus one. Data from HD BM spatial proteomics. J) Computational diagram. K) Scaled enrichment scores of cell types (x-axis) in ASC subset (y-axis) niches by individual (panel). Q-values<0.1 were colored white. Data from HD BM spatial proteomics. L) Representative images (panels) of ASC-rich regions colored by fluorescence signal (left) or cell type labels of segmented cells (right). Data from HD BM spatial proteomics.

Journal: bioRxiv

Article Title: Multi-omic profiling of human antibody-secreting cells reveals diverse subsets sustain durable humoral immunity

doi: 10.64898/2026.04.13.717827

Figure Lengend Snippet: A) Experimental diagram. B) wnnUMAPs of ASCs colored by tissue (left) or subset (right). Data from HD matched fixed CITEseq. C) Percent subset of total ASCs by sample. Data from HD matched fixed CITEseq. D) Percent subisotype usage by sample. Data from HD matched fixed CITEseq. E) Experimental diagram. F) Representative region of interest from a bone marrow core colored by fluorescence signal (top) or subset labels of segmented cells (bottom). Data from HD BM spatial proteomics. G) Percent ASC subset of total cells by individual. Data from HD BM spatial proteomics. H) Computational diagram. I) Observed (black diamond) and randomly permuted (grey density) percent of ASCs found in homotypic niches (defined as all ASCs in a niche having identical subset identities), by individual. Empirical p-values calculated as the number of permutations with homotypic niche frequencies greater or equal to the observed homotypic niche frequency, divided by the number of permutations plus one. Data from HD BM spatial proteomics. J) Computational diagram. K) Scaled enrichment scores of cell types (x-axis) in ASC subset (y-axis) niches by individual (panel). Q-values<0.1 were colored white. Data from HD BM spatial proteomics. L) Representative images (panels) of ASC-rich regions colored by fluorescence signal (left) or cell type labels of segmented cells (right). Data from HD BM spatial proteomics.

Article Snippet: For the ASC culture condition screen, total BM ASCs were stimulated for 72 hours with CpG ODN 2006 (10μg/mL, Invivogen) or BCR crosslinker (anti-kappa light chain; 1μg/mL, Southern Biotech) with various combinations of stimulatory reagents, including MEGACD40L (0.1μg/ml, Enzo Life Sciences), BAFF (1μg/mL, PeproTech), CXCL12 (0.1μg/ml, R&D Systems), IL-2 (0.1μg/mL, Biolegend), and IL-21 (0.1μg/mL, PeproTech).

Techniques: Fluorescence, Spatial Proteomics

A) Experimental diagram. B) Serum Ig concentrations of patients with NDMM by timepoint (x-axis), isotype (y-axis), and the isotype of each patient’s malignant cell (shapes). Transparency indicates values outside the healthy reference ranges specified in the clinical reports. Data from clinical quantitative Ig assay. C) Percent ASCs of total BMMCs for HDs (left) and patients with NDMM, by timepoint (x-axis). Crossbar indicates mean. Q-values calculated by Wilcoxon rank sum test with FDR correction, comparing to HDs. Data from MM longitudinal BM CITEseq. *Q<0.1; **Q<0.01; ***Q<0.001 D) Percent non-malignant ASCs of total ASCs for patients with NDMM, by timepoint (x-axis). Crossbar indicates mean. Q-values calculated by Wilcoxon rank sum test with FDR correction, comparing to PRETX. Data from MM longitudinal BM CITEseq. ***Q<0.001 E) Percent non-malignant ASC subset of total BMMCs for HDs (left) and patients with NDMM, by timepoint (x-axis) and subset (panels). Crossbar indicates mean. Q-values calculated by Wilcoxon rank sum test with FDR correction, comparing to HDs. Data from MM longitudinal BM CITEseq. *Q<0.1; **Q<0.01; ***Q<0.001

Journal: bioRxiv

Article Title: Multi-omic profiling of human antibody-secreting cells reveals diverse subsets sustain durable humoral immunity

doi: 10.64898/2026.04.13.717827

Figure Lengend Snippet: A) Experimental diagram. B) Serum Ig concentrations of patients with NDMM by timepoint (x-axis), isotype (y-axis), and the isotype of each patient’s malignant cell (shapes). Transparency indicates values outside the healthy reference ranges specified in the clinical reports. Data from clinical quantitative Ig assay. C) Percent ASCs of total BMMCs for HDs (left) and patients with NDMM, by timepoint (x-axis). Crossbar indicates mean. Q-values calculated by Wilcoxon rank sum test with FDR correction, comparing to HDs. Data from MM longitudinal BM CITEseq. *Q<0.1; **Q<0.01; ***Q<0.001 D) Percent non-malignant ASCs of total ASCs for patients with NDMM, by timepoint (x-axis). Crossbar indicates mean. Q-values calculated by Wilcoxon rank sum test with FDR correction, comparing to PRETX. Data from MM longitudinal BM CITEseq. ***Q<0.001 E) Percent non-malignant ASC subset of total BMMCs for HDs (left) and patients with NDMM, by timepoint (x-axis) and subset (panels). Crossbar indicates mean. Q-values calculated by Wilcoxon rank sum test with FDR correction, comparing to HDs. Data from MM longitudinal BM CITEseq. *Q<0.1; **Q<0.01; ***Q<0.001

Article Snippet: For the ASC culture condition screen, total BM ASCs were stimulated for 72 hours with CpG ODN 2006 (10μg/mL, Invivogen) or BCR crosslinker (anti-kappa light chain; 1μg/mL, Southern Biotech) with various combinations of stimulatory reagents, including MEGACD40L (0.1μg/ml, Enzo Life Sciences), BAFF (1μg/mL, PeproTech), CXCL12 (0.1μg/ml, R&D Systems), IL-2 (0.1μg/mL, Biolegend), and IL-21 (0.1μg/mL, PeproTech).

Techniques: