pro collagen i alpha 1 antibody Search Results


col 1  (R&D Systems)
99
R&D Systems col 1
Col 1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/col 1/product/R&D Systems
Average 99 stars, based on 1 article reviews
col 1 - by Bioz Stars, 2026-03
99/100 stars
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col1  (MedChemExpress)
94
MedChemExpress col1
Biological functional analysis of tri-layer scaffold systems. A) Representative images of migrated cells stained with crystal violet at 48 h. B) Number of migrating cells in control and CE-SKP. C) Glycosaminoglycan concentrations in control and CE-SKP at 7 and 14 days. D) qPCR analysis for COL2, SOX9, and ACAN. E) Western blotting of COL2 and SOX9. F) Alizarin red staining of control and CPH. G) ALP activity of control and CPH. H) qPCR analysis for <t>COL1,</t> COL10, OCN, and RUNX2. I) Western blotting of COL10, COL1, and RUNX2. J) Representative images of migrated cells stained with crystal violet at 48 h. K) Number of migrating cells in control and P2G3. L) Scanning electron microscope micrographs of P2G3. ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001.
Col1, supplied by MedChemExpress, 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/result/col1/product/MedChemExpress
Average 94 stars, based on 1 article reviews
col1 - by Bioz Stars, 2026-03
94/100 stars
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procollagen i  (R&D Systems)
93
R&D Systems procollagen i
Biological functional analysis of tri-layer scaffold systems. A) Representative images of migrated cells stained with crystal violet at 48 h. B) Number of migrating cells in control and CE-SKP. C) Glycosaminoglycan concentrations in control and CE-SKP at 7 and 14 days. D) qPCR analysis for COL2, SOX9, and ACAN. E) Western blotting of COL2 and SOX9. F) Alizarin red staining of control and CPH. G) ALP activity of control and CPH. H) qPCR analysis for <t>COL1,</t> COL10, OCN, and RUNX2. I) Western blotting of COL10, COL1, and RUNX2. J) Representative images of migrated cells stained with crystal violet at 48 h. K) Number of migrating cells in control and P2G3. L) Scanning electron microscope micrographs of P2G3. ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001.
Procollagen I, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/procollagen i/product/R&D Systems
Average 93 stars, based on 1 article reviews
procollagen i - by Bioz Stars, 2026-03
93/100 stars
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collagen i alpha i antibody  (R&D Systems)
94
R&D Systems collagen i alpha i antibody
Biological functional analysis of tri-layer scaffold systems. A) Representative images of migrated cells stained with crystal violet at 48 h. B) Number of migrating cells in control and CE-SKP. C) Glycosaminoglycan concentrations in control and CE-SKP at 7 and 14 days. D) qPCR analysis for COL2, SOX9, and ACAN. E) Western blotting of COL2 and SOX9. F) Alizarin red staining of control and CPH. G) ALP activity of control and CPH. H) qPCR analysis for <t>COL1,</t> COL10, OCN, and RUNX2. I) Western blotting of COL10, COL1, and RUNX2. J) Representative images of migrated cells stained with crystal violet at 48 h. K) Number of migrating cells in control and P2G3. L) Scanning electron microscope micrographs of P2G3. ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001.
Collagen I Alpha I Antibody, 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
https://www.bioz.com/result/collagen i alpha i antibody/product/R&D Systems
Average 94 stars, based on 1 article reviews
collagen i alpha i antibody - by Bioz Stars, 2026-03
94/100 stars
  Buy from Supplier
col1a1  (R&D Systems)
93
R&D Systems col1a1
Functional and structural changes to eLivs after neutron exposures. A) Schematic of the platform with eLiv tissue being characterized. B) Histological staining of eLivs using canonical markers for hepatocytes (CYP450, CK18), fibroblasts (vimentin), and matrix deposition <t>(COL1A1).</t> C) Albumin and D) urea secretion in eLiv culture supernatant, normalized to the untreated controls. E) Cytokine secretion by eLivs 24 h, 1 week, and 2 weeks post initial radiation exposure, normalized to the untreated controls. Significance was noted by two‐way ANOVAs with multiple comparisons.
Col1a1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/col1a1/product/R&D Systems
Average 93 stars, based on 1 article reviews
col1a1 - by Bioz Stars, 2026-03
93/100 stars
  Buy from Supplier

Image Search Results


Biological functional analysis of tri-layer scaffold systems. A) Representative images of migrated cells stained with crystal violet at 48 h. B) Number of migrating cells in control and CE-SKP. C) Glycosaminoglycan concentrations in control and CE-SKP at 7 and 14 days. D) qPCR analysis for COL2, SOX9, and ACAN. E) Western blotting of COL2 and SOX9. F) Alizarin red staining of control and CPH. G) ALP activity of control and CPH. H) qPCR analysis for COL1, COL10, OCN, and RUNX2. I) Western blotting of COL10, COL1, and RUNX2. J) Representative images of migrated cells stained with crystal violet at 48 h. K) Number of migrating cells in control and P2G3. L) Scanning electron microscope micrographs of P2G3. ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001.

Journal: Bioactive Materials

Article Title: Bioinspired scaffold recapitulating chondrogenic ontogeny and microenvironment for functional cartilage regeneration

doi: 10.1016/j.bioactmat.2025.11.041

Figure Lengend Snippet: Biological functional analysis of tri-layer scaffold systems. A) Representative images of migrated cells stained with crystal violet at 48 h. B) Number of migrating cells in control and CE-SKP. C) Glycosaminoglycan concentrations in control and CE-SKP at 7 and 14 days. D) qPCR analysis for COL2, SOX9, and ACAN. E) Western blotting of COL2 and SOX9. F) Alizarin red staining of control and CPH. G) ALP activity of control and CPH. H) qPCR analysis for COL1, COL10, OCN, and RUNX2. I) Western blotting of COL10, COL1, and RUNX2. J) Representative images of migrated cells stained with crystal violet at 48 h. K) Number of migrating cells in control and P2G3. L) Scanning electron microscope micrographs of P2G3. ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001.

Article Snippet: To evaluate the regeneration of cartilage, COL1 (1:100, HY- P81227 , MCE), COL2 (1:100, ARG20787 , Arigobio), and COL10 (1:100, BA2023, Boster) were used as a marker in immunohistochemistry (IHC) staining.

Techniques: Functional Assay, Staining, Control, Western Blot, Activity Assay, Microscopy

Regeneration of the femoral trochlea in a rabbit model. Representative images of IHC staining for A) COL1, B) COL10.

Journal: Bioactive Materials

Article Title: Bioinspired scaffold recapitulating chondrogenic ontogeny and microenvironment for functional cartilage regeneration

doi: 10.1016/j.bioactmat.2025.11.041

Figure Lengend Snippet: Regeneration of the femoral trochlea in a rabbit model. Representative images of IHC staining for A) COL1, B) COL10.

Article Snippet: To evaluate the regeneration of cartilage, COL1 (1:100, HY- P81227 , MCE), COL2 (1:100, ARG20787 , Arigobio), and COL10 (1:100, BA2023, Boster) were used as a marker in immunohistochemistry (IHC) staining.

Techniques: Immunohistochemistry

Functional and structural changes to eLivs after neutron exposures. A) Schematic of the platform with eLiv tissue being characterized. B) Histological staining of eLivs using canonical markers for hepatocytes (CYP450, CK18), fibroblasts (vimentin), and matrix deposition (COL1A1). C) Albumin and D) urea secretion in eLiv culture supernatant, normalized to the untreated controls. E) Cytokine secretion by eLivs 24 h, 1 week, and 2 weeks post initial radiation exposure, normalized to the untreated controls. Significance was noted by two‐way ANOVAs with multiple comparisons.

Journal: Advanced Science

Article Title: Modeling the Effects of Protracted Cosmic Radiation in a Human Organ‐on‐Chip Platform

doi: 10.1002/advs.202401415

Figure Lengend Snippet: Functional and structural changes to eLivs after neutron exposures. A) Schematic of the platform with eLiv tissue being characterized. B) Histological staining of eLivs using canonical markers for hepatocytes (CYP450, CK18), fibroblasts (vimentin), and matrix deposition (COL1A1). C) Albumin and D) urea secretion in eLiv culture supernatant, normalized to the untreated controls. E) Cytokine secretion by eLivs 24 h, 1 week, and 2 weeks post initial radiation exposure, normalized to the untreated controls. Significance was noted by two‐way ANOVAs with multiple comparisons.

Article Snippet: [ ] Sections were washed and permeabilized with 0.25% Triton‐X, blocked in 10% serum, and stained with tissue‐specific primary antibodies. eBM tissues were stained with CD45 (Mouse, AB1430). eLiv tissues were stained with Vimentin (Abcam, ab24525), CK18 (ReVMaB, 31‐1162‐00), anti‐cytochrome P450 CYP3A4 (Sigma, AB1254), COL1A1 (R&D Systems, MAB6220‐100), and ProLong Diamond Antifade Mountant with DAPI (ThermoFisher, P36962).

Techniques: Functional Assay, Staining