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c peptide levels  (ALPCO)


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    Structured Review

    ALPCO c peptide levels
    C Peptide Levels, supplied by ALPCO, used in various techniques. Bioz Stars score: 94/100, based on 320 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/c+peptide+levels/C-Peptide+ELISA/bio_rxiv__64898__2025__12__28__696610-119-3-15
    Average 94 stars, based on 320 article reviews
    c peptide levels - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Clinical Proteomics:

    Article Title: A glucose-sensing mechanism with glucose transporter 1 and pyruvate kinase in the area postrema regulates hepatic glucose production in rats.
    Article Snippet: .. Plasma samples were collected every 10 min into heparinized tubes and centrifuged for 30 s for the determination of [3-3H]glucose–specific activity, plasma glucose levels, and C-peptide levels (Alpco, rat ELISA c-peptide kit). .. Plasma glucose levels were determined by glucose oxidase method using a GM9 glucose analyzer (Analox Instruments).

    Article Title: Loss of Exocytosis Protein DOC2B is an Early Event in Type 1 Diabetes Development
    Article Snippet: At seven weeks of age, morning blood glucose levels were measured at 0800 hour using the Alphatrak2 glucose meter from Zoetis (Parsippany, NJ, USA), and then whole blood was collected from the retro-orbital sinus of NOD and NOR mice using EDTA-coated whole blood tubes. .. Following plasma separation, C-peptide levels were measured using a mouse C-peptide ELISA kit purchased from ALPCO (Salem, NH, USA, cat# 80-cptms-e01), according to the manufacturer’s instruction. ..

    Activity Assay:

    Article Title: A glucose-sensing mechanism with glucose transporter 1 and pyruvate kinase in the area postrema regulates hepatic glucose production in rats.
    Article Snippet: .. Plasma samples were collected every 10 min into heparinized tubes and centrifuged for 30 s for the determination of [3-3H]glucose–specific activity, plasma glucose levels, and C-peptide levels (Alpco, rat ELISA c-peptide kit). .. Plasma glucose levels were determined by glucose oxidase method using a GM9 glucose analyzer (Analox Instruments).

    Enzyme-linked Immunosorbent Assay:

    Article Title: A glucose-sensing mechanism with glucose transporter 1 and pyruvate kinase in the area postrema regulates hepatic glucose production in rats.
    Article Snippet: .. Plasma samples were collected every 10 min into heparinized tubes and centrifuged for 30 s for the determination of [3-3H]glucose–specific activity, plasma glucose levels, and C-peptide levels (Alpco, rat ELISA c-peptide kit). .. Plasma glucose levels were determined by glucose oxidase method using a GM9 glucose analyzer (Analox Instruments).

    Article Title: Insulin feedback is a targetable resistance mechanism of PI3K inhibition in glioblastoma.
    Article Snippet: Insulin levels were measured by ELISA (ALPCO, 80-INSMS-E01) from 5 μL of mouse serum collected 30 minutes after PI3K inhibitor treatment. .. C-peptide levels were measured by ELISA (ALPCO, 80-CPTMS-E01) from 5 μL of mouse serum collected 30 minutes after PI3K inhibitor treatment. .. Bioluminescence Mice were injected subcutaneously with 200 μL d-luciferin (150 mg/kg) and subjected to bioluminescence imaging using an IVIS CT Spectrum instrument (Perkin Elmer) at Day 7.

    Article Title: Checkpoint kinase 2 controls insulin secretion and glucose homeostasis
    Article Snippet: .. At the end of each stimulation, 100 μl buffer was collected to assess insulin or C-peptide levels with ELISA kits (Alpco and Novus Biologicals). .. The islet perifusion experiment was carried out in a BioRep Perifusion System.

    Article Title: Enhancing differentiation and functionality of insulin-producing cells derived from iPSCs using esterified collagen hydrogel for cell therapy in diabetes mellitus.
    Article Snippet: Samples were imaged using the EVOS® FL Auto Cell Imaging System (Thermo Fisher Scientific). .. Insulin and C-peptide levels were quantified using ELISA kits (Alpco, NH, USA; Mercodia, Uppsala, Sweden) according to the manufacturers’ protocols. ..

    Article Title: Loss of Exocytosis Protein DOC2B is an Early Event in Type 1 Diabetes Development
    Article Snippet: At seven weeks of age, morning blood glucose levels were measured at 0800 hour using the Alphatrak2 glucose meter from Zoetis (Parsippany, NJ, USA), and then whole blood was collected from the retro-orbital sinus of NOD and NOR mice using EDTA-coated whole blood tubes. .. Following plasma separation, C-peptide levels were measured using a mouse C-peptide ELISA kit purchased from ALPCO (Salem, NH, USA, cat# 80-cptms-e01), according to the manufacturer’s instruction. ..

    Article Title: Enhancing differentiation and functionality of insulin-producing cells derived from iPSCs using esterified collagen hydrogel for cell therapy in diabetes mellitus
    Article Snippet: Samples were imaged using the EVOS FL Auto Cell Imaging System (Thermo Fisher Scientific). .. Insulin and C-peptide levels were quantified using ELISA kits (Alpco, NH, USA; Mercodia, Uppsala, Sweden) according to the manufacturers’ protocols. ..

    Article Title: Checkpoint kinase 2 controls insulin secretion and glucose homeostasis.
    Article Snippet: .. At the end of each stimulation, 100 μl buffer was collected to assess insulin or C-peptide levels with ELISA kits (Alpco and Novus Biologicals). .. The islet perifusion experiment was carried out in a BioRep Perifusion System.

    other:

    Article Title: NSG mice lacking MHC class I and class II
    Article Snippet: Total insulin content within transplanted spleens was determined as previously described (Harlan D M, et al., 1995, Diabetes, 44:816-823) using an ELISA kit specific for human insulin (Alpco, Salem, N.H.). dsAAV Vectors The dsAAV vectors were engineered and packaged as previously described He Y, et al., 2013, Hum.



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    94
    R&D Systems human c peptide levels
    Secretion of therapeutic proteins with a-BLAST and d-BLAST. (a) The human preproinsulin (preproINS) construct contains a signal peptide, B-chain <t>(yellow),</t> <t>C-peptide</t> (dark gray), and A-chain (yellow), with engineered Furin cleavage sites flanking the C-peptide for maturation. To facilitate efficient processing within the Golgi apparatus, Furin protease was co-transfected with the BLAST modules. (b) Kinetic profiling of light-induced insulin secretion. Summary graphs of secreted C-peptide levels, quantified by ELISA, as a proxy for insulin secretion from a-BLAST (left) and d-BLAST (right). Both systems exhibited significant, time-dependent insulin release starting from 2 h of illumination (8.2-fold for a-BLAST, 8.4-fold for d-BLAST), reaching maximal induction at 24 h (13.8-fold for a-BLAST, 19.3-fold for d-BLAST). (c) Plasmid configurations for IL-12 secretion. Schematic of the heterodimeric cytokine IL-12-a-BLAST (left) and d-BLAST-IL-12 (right) constructs. (d) Kinetic profiling of light-induced IL-12 secretion. Summary graphs showing IL-12 secretion levels measured by ELISA. Significant secretion was observed starting at 3 h for a-BLAST (2.5-fold) and 2 h for d-BLAST (2.2-fold). At the 24 h time point, d-BLAST (4.7-fold) demonstrated a slightly higher dynamic range compared to a-BLAST (4.5-fold). Open circles represent individual measurements from three biologically independent samples. Data are presented as means ± S.D. Statistical significance was assessed using one-way ANOVA followed by Tukey’s multiple comparisons test (ns = not significant, * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001).
    Human C Peptide Levels, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ALPCO c peptide levels
    Secretion of therapeutic proteins with a-BLAST and d-BLAST. (a) The human preproinsulin (preproINS) construct contains a signal peptide, B-chain <t>(yellow),</t> <t>C-peptide</t> (dark gray), and A-chain (yellow), with engineered Furin cleavage sites flanking the C-peptide for maturation. To facilitate efficient processing within the Golgi apparatus, Furin protease was co-transfected with the BLAST modules. (b) Kinetic profiling of light-induced insulin secretion. Summary graphs of secreted C-peptide levels, quantified by ELISA, as a proxy for insulin secretion from a-BLAST (left) and d-BLAST (right). Both systems exhibited significant, time-dependent insulin release starting from 2 h of illumination (8.2-fold for a-BLAST, 8.4-fold for d-BLAST), reaching maximal induction at 24 h (13.8-fold for a-BLAST, 19.3-fold for d-BLAST). (c) Plasmid configurations for IL-12 secretion. Schematic of the heterodimeric cytokine IL-12-a-BLAST (left) and d-BLAST-IL-12 (right) constructs. (d) Kinetic profiling of light-induced IL-12 secretion. Summary graphs showing IL-12 secretion levels measured by ELISA. Significant secretion was observed starting at 3 h for a-BLAST (2.5-fold) and 2 h for d-BLAST (2.2-fold). At the 24 h time point, d-BLAST (4.7-fold) demonstrated a slightly higher dynamic range compared to a-BLAST (4.5-fold). Open circles represent individual measurements from three biologically independent samples. Data are presented as means ± S.D. Statistical significance was assessed using one-way ANOVA followed by Tukey’s multiple comparisons test (ns = not significant, * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001).
    C Peptide Levels, supplied by ALPCO, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/c+peptide+levels/C-Peptide+ELISA/bio_rxiv__64898__2025__12__28__696610-119-3-15
    Average 94 stars, based on 1 article reviews
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    Thermo Fisher c peptide level
    Secretion of therapeutic proteins with a-BLAST and d-BLAST. (a) The human preproinsulin (preproINS) construct contains a signal peptide, B-chain <t>(yellow),</t> <t>C-peptide</t> (dark gray), and A-chain (yellow), with engineered Furin cleavage sites flanking the C-peptide for maturation. To facilitate efficient processing within the Golgi apparatus, Furin protease was co-transfected with the BLAST modules. (b) Kinetic profiling of light-induced insulin secretion. Summary graphs of secreted C-peptide levels, quantified by ELISA, as a proxy for insulin secretion from a-BLAST (left) and d-BLAST (right). Both systems exhibited significant, time-dependent insulin release starting from 2 h of illumination (8.2-fold for a-BLAST, 8.4-fold for d-BLAST), reaching maximal induction at 24 h (13.8-fold for a-BLAST, 19.3-fold for d-BLAST). (c) Plasmid configurations for IL-12 secretion. Schematic of the heterodimeric cytokine IL-12-a-BLAST (left) and d-BLAST-IL-12 (right) constructs. (d) Kinetic profiling of light-induced IL-12 secretion. Summary graphs showing IL-12 secretion levels measured by ELISA. Significant secretion was observed starting at 3 h for a-BLAST (2.5-fold) and 2 h for d-BLAST (2.2-fold). At the 24 h time point, d-BLAST (4.7-fold) demonstrated a slightly higher dynamic range compared to a-BLAST (4.5-fold). Open circles represent individual measurements from three biologically independent samples. Data are presented as means ± S.D. Statistical significance was assessed using one-way ANOVA followed by Tukey’s multiple comparisons test (ns = not significant, * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001).
    C Peptide Level, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ALPCO mouse c peptide levels
    Secretion of therapeutic proteins with a-BLAST and d-BLAST. (a) The human preproinsulin (preproINS) construct contains a signal peptide, B-chain <t>(yellow),</t> <t>C-peptide</t> (dark gray), and A-chain (yellow), with engineered Furin cleavage sites flanking the C-peptide for maturation. To facilitate efficient processing within the Golgi apparatus, Furin protease was co-transfected with the BLAST modules. (b) Kinetic profiling of light-induced insulin secretion. Summary graphs of secreted C-peptide levels, quantified by ELISA, as a proxy for insulin secretion from a-BLAST (left) and d-BLAST (right). Both systems exhibited significant, time-dependent insulin release starting from 2 h of illumination (8.2-fold for a-BLAST, 8.4-fold for d-BLAST), reaching maximal induction at 24 h (13.8-fold for a-BLAST, 19.3-fold for d-BLAST). (c) Plasmid configurations for IL-12 secretion. Schematic of the heterodimeric cytokine IL-12-a-BLAST (left) and d-BLAST-IL-12 (right) constructs. (d) Kinetic profiling of light-induced IL-12 secretion. Summary graphs showing IL-12 secretion levels measured by ELISA. Significant secretion was observed starting at 3 h for a-BLAST (2.5-fold) and 2 h for d-BLAST (2.2-fold). At the 24 h time point, d-BLAST (4.7-fold) demonstrated a slightly higher dynamic range compared to a-BLAST (4.5-fold). Open circles represent individual measurements from three biologically independent samples. Data are presented as means ± S.D. Statistical significance was assessed using one-way ANOVA followed by Tukey’s multiple comparisons test (ns = not significant, * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001).
    Mouse C Peptide Levels, supplied by ALPCO, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore insulin, c-peptide, and incretin hormone levels
    Secretion of therapeutic proteins with a-BLAST and d-BLAST. (a) The human preproinsulin (preproINS) construct contains a signal peptide, B-chain <t>(yellow),</t> <t>C-peptide</t> (dark gray), and A-chain (yellow), with engineered Furin cleavage sites flanking the C-peptide for maturation. To facilitate efficient processing within the Golgi apparatus, Furin protease was co-transfected with the BLAST modules. (b) Kinetic profiling of light-induced insulin secretion. Summary graphs of secreted C-peptide levels, quantified by ELISA, as a proxy for insulin secretion from a-BLAST (left) and d-BLAST (right). Both systems exhibited significant, time-dependent insulin release starting from 2 h of illumination (8.2-fold for a-BLAST, 8.4-fold for d-BLAST), reaching maximal induction at 24 h (13.8-fold for a-BLAST, 19.3-fold for d-BLAST). (c) Plasmid configurations for IL-12 secretion. Schematic of the heterodimeric cytokine IL-12-a-BLAST (left) and d-BLAST-IL-12 (right) constructs. (d) Kinetic profiling of light-induced IL-12 secretion. Summary graphs showing IL-12 secretion levels measured by ELISA. Significant secretion was observed starting at 3 h for a-BLAST (2.5-fold) and 2 h for d-BLAST (2.2-fold). At the 24 h time point, d-BLAST (4.7-fold) demonstrated a slightly higher dynamic range compared to a-BLAST (4.5-fold). Open circles represent individual measurements from three biologically independent samples. Data are presented as means ± S.D. Statistical significance was assessed using one-way ANOVA followed by Tukey’s multiple comparisons test (ns = not significant, * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001).
    Insulin, C Peptide, And Incretin Hormone Levels, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Roche fasting c peptide levels
    The relationship between the variant rs912304 and residual islet function and islet autoimmunity in T1D individuals. A - C The association between rs912304 and fasting C-peptide level in total newly diagnosed T1D subjects, those diagnosed age <12 and ≥12 years old, respectively. D - F The association between rs912304 and 2-hour C-peptide AUC in total newly diagnosed T1D subjects, those diagnosed age <12 and ≥12 years old, respectively. G - I The association between rs912304 and the positive rate of ZnT8A, GADA, and IA-2A in total T1D subjects. The genotype distribution of rs912304 in newly diagnosed T1D subjects: GG = 52, TG = 102, TT = 48; T1D subjects with diagnosed age <12: GG = 10, TG = 26, TT = 8; and T1D subjects with diagnosed age ≥12: GG = 42, TG = 76, TT = 40. The genotype distribution of rs912304 in islet autoimmunity: GG=616, GT=1004, TT=420 for ZnT8A; GG=644, GT=1061, TT=443 for GADA; GG=639, GT=1059, TT=443 for IA-2A. The above correlations were analyzed by linear regression analysis and were corrected for sex and duration of T1D disease. Data are mean with 95%CI. * P <0.05 was considered as significant
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    TaKaRa pip levels
    Fig. 5. Procollagen type I C-peptide <t>(PIP)</t> <t>levels</t> in HDF culture medium supernatants 24 hr after treatment with glycoside-rich C. asiatica extracts (GRCs) at various concentrations (0.1, 1, and 10 µg/ml). *p < 0.05 vs. 1 % DMSO (control).
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    ALPCO plasma c peptide levels
    Fig. 5. Procollagen type I C-peptide <t>(PIP)</t> <t>levels</t> in HDF culture medium supernatants 24 hr after treatment with glycoside-rich C. asiatica extracts (GRCs) at various concentrations (0.1, 1, and 10 µg/ml). *p < 0.05 vs. 1 % DMSO (control).
    Plasma C Peptide Levels, supplied by ALPCO, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Secretion of therapeutic proteins with a-BLAST and d-BLAST. (a) The human preproinsulin (preproINS) construct contains a signal peptide, B-chain (yellow), C-peptide (dark gray), and A-chain (yellow), with engineered Furin cleavage sites flanking the C-peptide for maturation. To facilitate efficient processing within the Golgi apparatus, Furin protease was co-transfected with the BLAST modules. (b) Kinetic profiling of light-induced insulin secretion. Summary graphs of secreted C-peptide levels, quantified by ELISA, as a proxy for insulin secretion from a-BLAST (left) and d-BLAST (right). Both systems exhibited significant, time-dependent insulin release starting from 2 h of illumination (8.2-fold for a-BLAST, 8.4-fold for d-BLAST), reaching maximal induction at 24 h (13.8-fold for a-BLAST, 19.3-fold for d-BLAST). (c) Plasmid configurations for IL-12 secretion. Schematic of the heterodimeric cytokine IL-12-a-BLAST (left) and d-BLAST-IL-12 (right) constructs. (d) Kinetic profiling of light-induced IL-12 secretion. Summary graphs showing IL-12 secretion levels measured by ELISA. Significant secretion was observed starting at 3 h for a-BLAST (2.5-fold) and 2 h for d-BLAST (2.2-fold). At the 24 h time point, d-BLAST (4.7-fold) demonstrated a slightly higher dynamic range compared to a-BLAST (4.5-fold). Open circles represent individual measurements from three biologically independent samples. Data are presented as means ± S.D. Statistical significance was assessed using one-way ANOVA followed by Tukey’s multiple comparisons test (ns = not significant, * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001).

    Journal: bioRxiv

    Article Title: BLAST: A blue light-assisted secretion toolkit tunable by reversible protein-protein interactions

    doi: 10.64898/2026.03.30.715452

    Figure Lengend Snippet: Secretion of therapeutic proteins with a-BLAST and d-BLAST. (a) The human preproinsulin (preproINS) construct contains a signal peptide, B-chain (yellow), C-peptide (dark gray), and A-chain (yellow), with engineered Furin cleavage sites flanking the C-peptide for maturation. To facilitate efficient processing within the Golgi apparatus, Furin protease was co-transfected with the BLAST modules. (b) Kinetic profiling of light-induced insulin secretion. Summary graphs of secreted C-peptide levels, quantified by ELISA, as a proxy for insulin secretion from a-BLAST (left) and d-BLAST (right). Both systems exhibited significant, time-dependent insulin release starting from 2 h of illumination (8.2-fold for a-BLAST, 8.4-fold for d-BLAST), reaching maximal induction at 24 h (13.8-fold for a-BLAST, 19.3-fold for d-BLAST). (c) Plasmid configurations for IL-12 secretion. Schematic of the heterodimeric cytokine IL-12-a-BLAST (left) and d-BLAST-IL-12 (right) constructs. (d) Kinetic profiling of light-induced IL-12 secretion. Summary graphs showing IL-12 secretion levels measured by ELISA. Significant secretion was observed starting at 3 h for a-BLAST (2.5-fold) and 2 h for d-BLAST (2.2-fold). At the 24 h time point, d-BLAST (4.7-fold) demonstrated a slightly higher dynamic range compared to a-BLAST (4.5-fold). Open circles represent individual measurements from three biologically independent samples. Data are presented as means ± S.D. Statistical significance was assessed using one-way ANOVA followed by Tukey’s multiple comparisons test (ns = not significant, * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001).

    Article Snippet: Secreted human C-peptide levels in the supernatant were quantified using a Human C-peptide ELISA Kit (R&D Systems; Catalog #DICP00).

    Techniques: Construct, Transfection, Enzyme-linked Immunosorbent Assay, Plasmid Preparation

    The relationship between the variant rs912304 and residual islet function and islet autoimmunity in T1D individuals. A - C The association between rs912304 and fasting C-peptide level in total newly diagnosed T1D subjects, those diagnosed age <12 and ≥12 years old, respectively. D - F The association between rs912304 and 2-hour C-peptide AUC in total newly diagnosed T1D subjects, those diagnosed age <12 and ≥12 years old, respectively. G - I The association between rs912304 and the positive rate of ZnT8A, GADA, and IA-2A in total T1D subjects. The genotype distribution of rs912304 in newly diagnosed T1D subjects: GG = 52, TG = 102, TT = 48; T1D subjects with diagnosed age <12: GG = 10, TG = 26, TT = 8; and T1D subjects with diagnosed age ≥12: GG = 42, TG = 76, TT = 40. The genotype distribution of rs912304 in islet autoimmunity: GG=616, GT=1004, TT=420 for ZnT8A; GG=644, GT=1061, TT=443 for GADA; GG=639, GT=1059, TT=443 for IA-2A. The above correlations were analyzed by linear regression analysis and were corrected for sex and duration of T1D disease. Data are mean with 95%CI. * P <0.05 was considered as significant

    Journal: BMC Medicine

    Article Title: A functional variant rs912304 for late-onset T1D risk contributes to islet dysfunction by regulating proinflammatory cytokine-responsive gene STXBP6 expression

    doi: 10.1186/s12916-024-03583-w

    Figure Lengend Snippet: The relationship between the variant rs912304 and residual islet function and islet autoimmunity in T1D individuals. A - C The association between rs912304 and fasting C-peptide level in total newly diagnosed T1D subjects, those diagnosed age <12 and ≥12 years old, respectively. D - F The association between rs912304 and 2-hour C-peptide AUC in total newly diagnosed T1D subjects, those diagnosed age <12 and ≥12 years old, respectively. G - I The association between rs912304 and the positive rate of ZnT8A, GADA, and IA-2A in total T1D subjects. The genotype distribution of rs912304 in newly diagnosed T1D subjects: GG = 52, TG = 102, TT = 48; T1D subjects with diagnosed age <12: GG = 10, TG = 26, TT = 8; and T1D subjects with diagnosed age ≥12: GG = 42, TG = 76, TT = 40. The genotype distribution of rs912304 in islet autoimmunity: GG=616, GT=1004, TT=420 for ZnT8A; GG=644, GT=1061, TT=443 for GADA; GG=639, GT=1059, TT=443 for IA-2A. The above correlations were analyzed by linear regression analysis and were corrected for sex and duration of T1D disease. Data are mean with 95%CI. * P <0.05 was considered as significant

    Article Snippet: This test was not required for T1D patients with fasting C-peptide levels ≤ 25 pmol/L, but only the fasting C-peptide level was measured by chemiluminescence (Roche Diagnostics, Switzerland).

    Techniques: Variant Assay

    Fig. 5. Procollagen type I C-peptide (PIP) levels in HDF culture medium supernatants 24 hr after treatment with glycoside-rich C. asiatica extracts (GRCs) at various concentrations (0.1, 1, and 10 µg/ml). *p < 0.05 vs. 1 % DMSO (control).

    Journal: Phytomedicine Plus

    Article Title: The effects of glycoside-rich green extract from Centella asiatica (L.) Urban on wound healing and anti-aging activity

    doi: 10.1016/j.phyplu.2024.100628

    Figure Lengend Snippet: Fig. 5. Procollagen type I C-peptide (PIP) levels in HDF culture medium supernatants 24 hr after treatment with glycoside-rich C. asiatica extracts (GRCs) at various concentrations (0.1, 1, and 10 µg/ml). *p < 0.05 vs. 1 % DMSO (control).

    Article Snippet: After 24 hr of incubation, the culture supernatants were collected, and the PIP levels were determined by following the PIP ELISA Kit protocol (MK101, Takara Bio, Inc.).

    Techniques: Control

    Fig. 6. Procollagen type I C-peptide (PIP) levels in HDF culture medium supernatants 24 hr after treatment with 10 µg/ml GRC1 and different components: total triterpenoids (MS+AS+MA+AA), glycosides (MS+AS), aglycones (MA+AA) and individual triterpenoids (MS, AS, MA, AA). *p < 0.05 vs. 1 % DMSO (control) #p < 0.05 vs. 10 µg/ml GRC1 MS=Madecassoside; AS=Asiaticoside; MA=Madecassic acid; AA=Asiatic acid.

    Journal: Phytomedicine Plus

    Article Title: The effects of glycoside-rich green extract from Centella asiatica (L.) Urban on wound healing and anti-aging activity

    doi: 10.1016/j.phyplu.2024.100628

    Figure Lengend Snippet: Fig. 6. Procollagen type I C-peptide (PIP) levels in HDF culture medium supernatants 24 hr after treatment with 10 µg/ml GRC1 and different components: total triterpenoids (MS+AS+MA+AA), glycosides (MS+AS), aglycones (MA+AA) and individual triterpenoids (MS, AS, MA, AA). *p < 0.05 vs. 1 % DMSO (control) #p < 0.05 vs. 10 µg/ml GRC1 MS=Madecassoside; AS=Asiaticoside; MA=Madecassic acid; AA=Asiatic acid.

    Article Snippet: After 24 hr of incubation, the culture supernatants were collected, and the PIP levels were determined by following the PIP ELISA Kit protocol (MK101, Takara Bio, Inc.).

    Techniques: Control