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recombinant human pro collagen col3a1  (R&D Systems)


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    Structured Review

    R&D Systems recombinant human pro collagen col3a1
    Transcripts With Altered Gene Expression in the EXP Compared to NORM
    Recombinant Human Pro Collagen Col3a1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/recombinant+human+pro+collagen+col3a1/Recombinant+Human+Pro-Collagen+III+alpha+1%2FCOL3A1%2C+CF/pmc10919888-109-13-17
    Average 92 stars, based on 5 article reviews
    recombinant human pro collagen col3a1 - by Bioz Stars, 2026-09
    92/100 stars

    Images

    1) Product Images from "Transcriptional Profiling of Muscle in Females With Distal Radius Fracture and Functional Sarcopenia"

    Article Title: Transcriptional Profiling of Muscle in Females With Distal Radius Fracture and Functional Sarcopenia

    Journal: The Journals of Gerontology Series A: Biological Sciences and Medical Sciences

    doi: 10.1093/gerona/glae002

    Transcripts With Altered Gene Expression in the EXP Compared to NORM
    Figure Legend Snippet: Transcripts With Altered Gene Expression in the EXP Compared to NORM

    Techniques Used: Gene Expression

    Related Articles

    Recombinant:

    Article Title: Transcriptional Profiling of Muscle in Females With Distal Radius Fracture and Functional Sarcopenia
    Article Snippet: .. Recombinant human pro-collagen COL1A1 (R&D System, Minneapolis, MN, USA, 6220-CL) 75 μg/mL and recombinant human pro-collagen COL3A1 (R&D System, 7294-CL) 75 μg/mL were incubated with 5 μg/mL recombinant human BMP-1 (R&D, 1927-ZN) for 2 hours. ..

    Incubation:

    Article Title: Transcriptional Profiling of Muscle in Females With Distal Radius Fracture and Functional Sarcopenia
    Article Snippet: .. Recombinant human pro-collagen COL1A1 (R&D System, Minneapolis, MN, USA, 6220-CL) 75 μg/mL and recombinant human pro-collagen COL3A1 (R&D System, 7294-CL) 75 μg/mL were incubated with 5 μg/mL recombinant human BMP-1 (R&D, 1927-ZN) for 2 hours. ..



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    R&D Systems recombinant human pro collagen col3a1
    Transcripts With Altered Gene Expression in the EXP Compared to NORM
    Recombinant Human Pro Collagen Col3a1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/recombinant+human+pro+collagen+col3a1/Recombinant+Human+Pro-Collagen+III+alpha+1%2FCOL3A1%2C+CF/pmc10919888-109-13-17
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    NPL1010 and NPL3008 rarely inhibit BMP1-dependent <t>COL3A1</t> cleavage. ( A ) COL3A1 cleavage assay. <t>rhCOL3A1</t> was incubated with rhBMP1. The effects of NPL1010 and NPL3008 on BMP1-dependent rhCOL3A1 cleavage were analyzed using SDS–PAGE and Oriole staining. Arrows indicate full-length rhCOL3A1 and cleaved rhCOL3A1. ( B ) Statistical analysis of BMP1-dependent cleavage of COL3A1. The levels of noncleaved and cleaved COL3A1 were measured by performing densitometry of the Oriole-stained gel, and the percentage of cleaved COL3A1 was calculated based on the fragments detected at each molecular weight and background. **: p < 0.01 (Dunnett’s test). The error bar indicates +s.d. with individual data shown ( n = 4).
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    Figure 6. NC410 <t>increases</t> <t>collagen</t> degradation products that correlate with tumor regression. (A) Schematic representation of the humanized murine tumor model used. HT-29 tumor was injected subcutaneously in the presence of human peripheral blood mononuclear cells. Mice were treated with NC410 or control by intraperitoneal injection, Q4D 4 doses followed by Q7D until endpoint. Mice were bled prior to start of experiment and weekly for 4 weeks. (B) Tumor growth kinetics with NC410. Asterisks indicate statistical significance: *p<0.05, ****p<0.0001, two-way ANOVA with Sidak multiple comparisons. (C) Analysis of collagen degradation products in serum at baseline, at weeks 1, 2, 3 and 4. reC1M: neo-epitope of MMP-2,9,13- mediated degradation of type I collagen; C3M: type <t>III</t> collagen degradation by MMP; C4M: type IV collagen degradation by MMP; C6M: neo-epitope of MMP-2-mediated degradation of type VI collagen; PRO-C3: pro-peptide of type III collagen/ECM formation/fibroblast activity; PRO-C6: pro-peptide of type VI collagen; VICM: neo-epitope of MMP-2,8, trypsin-mediated degradation of citrullinated vimentin; C4G: type IV collagen degraded by Figure 6 continued on next page
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    Figure 6. NC410 <t>increases</t> <t>collagen</t> degradation products that correlate with tumor regression. (A) Schematic representation of the humanized murine tumor model used. HT-29 tumor was injected subcutaneously in the presence of human peripheral blood mononuclear cells. Mice were treated with NC410 or control by intraperitoneal injection, Q4D 4 doses followed by Q7D until endpoint. Mice were bled prior to start of experiment and weekly for 4 weeks. (B) Tumor growth kinetics with NC410. Asterisks indicate statistical significance: *p<0.05, ****p<0.0001, two-way ANOVA with Sidak multiple comparisons. (C) Analysis of collagen degradation products in serum at baseline, at weeks 1, 2, 3 and 4. reC1M: neo-epitope of MMP-2,9,13- mediated degradation of type I collagen; C3M: type <t>III</t> collagen degradation by MMP; C4M: type IV collagen degradation by MMP; C6M: neo-epitope of MMP-2-mediated degradation of type VI collagen; PRO-C3: pro-peptide of type III collagen/ECM formation/fibroblast activity; PRO-C6: pro-peptide of type VI collagen; VICM: neo-epitope of MMP-2,8, trypsin-mediated degradation of citrullinated vimentin; C4G: type IV collagen degraded by Figure 6 continued on next page
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    Figure 6. NC410 <t>increases</t> <t>collagen</t> degradation products that correlate with tumor regression. (A) Schematic representation of the humanized murine tumor model used. HT-29 tumor was injected subcutaneously in the presence of human peripheral blood mononuclear cells. Mice were treated with NC410 or control by intraperitoneal injection, Q4D 4 doses followed by Q7D until endpoint. Mice were bled prior to start of experiment and weekly for 4 weeks. (B) Tumor growth kinetics with NC410. Asterisks indicate statistical significance: *p<0.05, ****p<0.0001, two-way ANOVA with Sidak multiple comparisons. (C) Analysis of collagen degradation products in serum at baseline, at weeks 1, 2, 3 and 4. reC1M: neo-epitope of MMP-2,9,13- mediated degradation of type I collagen; C3M: type <t>III</t> collagen degradation by MMP; C4M: type IV collagen degradation by MMP; C6M: neo-epitope of MMP-2-mediated degradation of type VI collagen; PRO-C3: pro-peptide of type III collagen/ECM formation/fibroblast activity; PRO-C6: pro-peptide of type VI collagen; VICM: neo-epitope of MMP-2,8, trypsin-mediated degradation of citrullinated vimentin; C4G: type IV collagen degraded by Figure 6 continued on next page
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    Image Search Results


    Transcripts With Altered Gene Expression in the EXP Compared to NORM

    Journal: The Journals of Gerontology Series A: Biological Sciences and Medical Sciences

    Article Title: Transcriptional Profiling of Muscle in Females With Distal Radius Fracture and Functional Sarcopenia

    doi: 10.1093/gerona/glae002

    Figure Lengend Snippet: Transcripts With Altered Gene Expression in the EXP Compared to NORM

    Article Snippet: Recombinant human pro-collagen COL1A1 (R&D System, Minneapolis, MN, USA, 6220-CL) 75 μg/mL and recombinant human pro-collagen COL3A1 (R&D System, 7294-CL) 75 μg/mL were incubated with 5 μg/mL recombinant human BMP-1 (R&D, 1927-ZN) for 2 hours.

    Techniques: Gene Expression

    NPL1010 and NPL3008 rarely inhibit BMP1-dependent COL3A1 cleavage. ( A ) COL3A1 cleavage assay. rhCOL3A1 was incubated with rhBMP1. The effects of NPL1010 and NPL3008 on BMP1-dependent rhCOL3A1 cleavage were analyzed using SDS–PAGE and Oriole staining. Arrows indicate full-length rhCOL3A1 and cleaved rhCOL3A1. ( B ) Statistical analysis of BMP1-dependent cleavage of COL3A1. The levels of noncleaved and cleaved COL3A1 were measured by performing densitometry of the Oriole-stained gel, and the percentage of cleaved COL3A1 was calculated based on the fragments detected at each molecular weight and background. **: p < 0.01 (Dunnett’s test). The error bar indicates +s.d. with individual data shown ( n = 4).

    Journal: International Journal of Molecular Sciences

    Article Title: Small-Molecule-Mediated Suppression of BMP Signaling by Selective Inhibition of BMP1-Dependent Chordin Cleavage

    doi: 10.3390/ijms24054313

    Figure Lengend Snippet: NPL1010 and NPL3008 rarely inhibit BMP1-dependent COL3A1 cleavage. ( A ) COL3A1 cleavage assay. rhCOL3A1 was incubated with rhBMP1. The effects of NPL1010 and NPL3008 on BMP1-dependent rhCOL3A1 cleavage were analyzed using SDS–PAGE and Oriole staining. Arrows indicate full-length rhCOL3A1 and cleaved rhCOL3A1. ( B ) Statistical analysis of BMP1-dependent cleavage of COL3A1. The levels of noncleaved and cleaved COL3A1 were measured by performing densitometry of the Oriole-stained gel, and the percentage of cleaved COL3A1 was calculated based on the fragments detected at each molecular weight and background. **: p < 0.01 (Dunnett’s test). The error bar indicates +s.d. with individual data shown ( n = 4).

    Article Snippet: Recombinant human BMP1 (rhBMP1, 0.276 mg/mL, dissolved in 25 mM HEPES containing 400 mM ammonium sulfate, R&D Systems, Minneapolis, MN, USA, catalog no. 1927-ZN-010) and recombinant human COL3A1 (rhCOL3A1, 0.336 mg/mL, dissolved in 25 mM sodium acetate containing 1 M NaCl, R&D Systems, catalog no. 7294-CL-020) were divided into aliquots and stored at −80 °C.

    Techniques: Cleavage Assay, Incubation, SDS Page, Staining, Molecular Weight

    Figure 6. NC410 increases collagen degradation products that correlate with tumor regression. (A) Schematic representation of the humanized murine tumor model used. HT-29 tumor was injected subcutaneously in the presence of human peripheral blood mononuclear cells. Mice were treated with NC410 or control by intraperitoneal injection, Q4D 4 doses followed by Q7D until endpoint. Mice were bled prior to start of experiment and weekly for 4 weeks. (B) Tumor growth kinetics with NC410. Asterisks indicate statistical significance: *p<0.05, ****p<0.0001, two-way ANOVA with Sidak multiple comparisons. (C) Analysis of collagen degradation products in serum at baseline, at weeks 1, 2, 3 and 4. reC1M: neo-epitope of MMP-2,9,13- mediated degradation of type I collagen; C3M: type III collagen degradation by MMP; C4M: type IV collagen degradation by MMP; C6M: neo-epitope of MMP-2-mediated degradation of type VI collagen; PRO-C3: pro-peptide of type III collagen/ECM formation/fibroblast activity; PRO-C6: pro-peptide of type VI collagen; VICM: neo-epitope of MMP-2,8, trypsin-mediated degradation of citrullinated vimentin; C4G: type IV collagen degraded by Figure 6 continued on next page

    Journal: eLife

    Article Title: Cancer immunotherapy by NC410, a LAIR-2 Fc protein blocking human LAIR-collagen interaction

    doi: 10.7554/elife.62927

    Figure Lengend Snippet: Figure 6. NC410 increases collagen degradation products that correlate with tumor regression. (A) Schematic representation of the humanized murine tumor model used. HT-29 tumor was injected subcutaneously in the presence of human peripheral blood mononuclear cells. Mice were treated with NC410 or control by intraperitoneal injection, Q4D 4 doses followed by Q7D until endpoint. Mice were bled prior to start of experiment and weekly for 4 weeks. (B) Tumor growth kinetics with NC410. Asterisks indicate statistical significance: *p<0.05, ****p<0.0001, two-way ANOVA with Sidak multiple comparisons. (C) Analysis of collagen degradation products in serum at baseline, at weeks 1, 2, 3 and 4. reC1M: neo-epitope of MMP-2,9,13- mediated degradation of type I collagen; C3M: type III collagen degradation by MMP; C4M: type IV collagen degradation by MMP; C6M: neo-epitope of MMP-2-mediated degradation of type VI collagen; PRO-C3: pro-peptide of type III collagen/ECM formation/fibroblast activity; PRO-C6: pro-peptide of type VI collagen; VICM: neo-epitope of MMP-2,8, trypsin-mediated degradation of citrullinated vimentin; C4G: type IV collagen degraded by Figure 6 continued on next page

    Article Snippet: The anti-human Fc antibody capture sensors (ForteBio) were first loaded with LAIR-2-Fc followed by an association step where the loaded sensor was dipped into wells containing human, mouse or rat collagen I (human, R&D Systems; mouse, Ray Biotech; rat, Yo Protein) or collagen III (human, R&D Systems; rat, Yo Protein).

    Techniques: Injection, Control, Activity Assay