Paper40870
Differential elution of Clq, Clr and Cls from human Cl bound to immune aggregates. Use in the rapid purification of Cl subcomponents.
Arlaud GJ and 3 others. Mol Immunol, 1979. Cited by 141 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
Cite this record
ConductScience Library. Differential elution of Clq, Clr and Cls from human Cl bound to immune aggregates. Use in the rapid purification of Cl subcomponents. Papers, record 40870. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/40870
Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- Differential elution of Clq, Clr and Cls from human Cl bound to immune aggregates. Use in the rapid purification of Cl subcomponents.
- PubMed
Topics9
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Complement C1 | Major topic |
| Complement Pathway, Classical | |
| Electrophoresis, Polyacrylamide Gel | |
| Humans | |
| Hydrogen-Ion Concentration | |
| Immunoglobulin G | |
| Osmolar Concentration | |
| Ovalbumin | |
| Protein Binding |
Source PubMed
Cited by51
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 141 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 41,176,693 | The fc fragment of IgMs binds C1q to activate the first step of the classical complement pathway, while inhibiting complement-dependent cytotoxicity. | FEBS J | 2026 | https://conductscience.org/library/papers/41176693 | PubMed |
| 38,911,852 | Revisiting the interaction between complement lectin pathway protease MASP-2 and SARS-CoV-2 nucleoprotein. | Front Immunol | 2024 | https://conductscience.org/library/papers/38911852 | PubMed |
| 35,685,087 | Biophysical Characterization of the Oligomeric States of Recombinant Immunoglobulins Type-M and Their C1q-Binding Kinetics by Biolayer Interferometry. | Front Bioeng Biotechnol | 2022 | https://conductscience.org/library/papers/35685087 | PubMed |
| 34,066,122 | Molecular Basis of Complement C1q Collagen-Like Region Interaction with the Immunoglobulin-Like Receptor LAIR-1. | Int J Mol Sci | 2021 | https://conductscience.org/library/papers/34066122 | PubMed |
| 33,193,398 | Complement C1q Interacts With LRP1 Clusters II and IV Through a Site Close but Different From the Binding Site of Its C1r and C1s-Associated Proteases. | Front Immunol | 2020 | https://conductscience.org/library/papers/33193398 | PubMed |
| 32,296,440 | Molecular and Cellular Interactions of Scavenger Receptor SR-F1 With Complement C1q Provide Insights Into Its Role in the Clearance of Apoptotic Cells. | Front Immunol | 2020 | https://conductscience.org/library/papers/32296440 | PubMed |
| 32,163,462 | Transient pentameric IgM fulfill biological function-Effect of expression host and transfection on IgM properties. | PLoS One | 2020 | https://conductscience.org/library/papers/32163462 | PubMed |
| 31,749,804 | C1R Mutations Trigger Constitutive Complement 1 Activation in Periodontal Ehlers-Danlos Syndrome. | Front Immunol | 2019 | https://conductscience.org/library/papers/31749804 | PubMed |
| 30,923,526 | Interaction of C1q With Pentraxin 3 and IgM Revisited: Mutational Studies With Recombinant C1q Variants. | Front Immunol | 2019 | https://conductscience.org/library/papers/30923526 | PubMed |
| 29,563,915 | C1q and Mannose-Binding Lectin Interact with CR1 in the Same Region on CCP24-25 Modules. | Front Immunol | 2018 | https://conductscience.org/library/papers/29563915 | PubMed |
| 29,209,066 | Interaction of Complement Defence Collagens C1q and Mannose-Binding Lectin with BMP-1/Tolloid-like Proteinases. | Sci Rep | 2017 | https://conductscience.org/library/papers/29209066 | PubMed |
| 26,973,654 | Structural and Functional Characterization of a Single-Chain Form of the Recognition Domain of Complement Protein C1q. | Front Immunol | 2016 | https://conductscience.org/library/papers/26973654 | PubMed |
| 23,861,840 | The serine protease domain of MASP-3: enzymatic properties and crystal structure in complex with ecotin. | PLoS One | 2013 | https://conductscience.org/library/papers/23861840 | PubMed |
| 23,650,384 | Expression of recombinant human complement C1q allows identification of the C1r/C1s-binding sites. | Proc Natl Acad Sci U S A | 2013 | https://conductscience.org/library/papers/23650384 | PubMed |
| 20,727,163 | Recombinant human complement component C2 produced in a human cell line restores the classical complement pathway activity in-vitro: an alternative treatment for C2 deficiency diseases. | BMC Immunol | 2010 | https://conductscience.org/library/papers/20727163 | PubMed |
| 20,592,021 | Mapping surface accessibility of the C1r/C1s tetramer by chemical modification and mass spectrometry provides new insights into assembly of the human C1 complex. | J Biol Chem | 2010 | https://conductscience.org/library/papers/20592021 | PubMed |
| 20,410,306 | Complement protein C1q forms a complex with cytotoxic prion protein oligomers. | J Biol Chem | 2010 | https://conductscience.org/library/papers/20410306 | PubMed |
| 20,008,834 | Analysis of human C1q by combined bottom-up and top-down mass spectrometry: detailed mapping of post-translational modifications and insights into the C1r/C1s binding sites. | Mol Cell Proteomics | 2010 | https://conductscience.org/library/papers/20008834 | PubMed |
| 19,494,295 | Analogous interactions in initiating complexes of the classical and lectin pathways of complement. | J Immunol | 2009 | https://conductscience.org/library/papers/19494295 | PubMed |
| 19,473,974 | Identification of the C1q-binding Sites of Human C1r and C1s: a refined three-dimensional model of the C1 complex of complement. | J Biol Chem | 2009 | https://conductscience.org/library/papers/19473974 | PubMed |
Data dates
The date of each source this release read.
- Trials
- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
None in this release
- Grants
- Trials
- Comments and corrections
- References
- Genes
- Drugs
- Data
Sources 11
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- HGNCCC0
- iCiteCC BY 4.0
- NCBI GenePublic domain (US government)
- NIH RePORTER's grant and paper linksPublic domain
- Open TargetsCC0 1.0
- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- HGNCCC0: https://www.genenames.org/about/license/
- iCiteCC BY 4.0
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this paper from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/papers/v1/40870
GET https://conductscience.org/api/papers/v1/40870/cited_by?page=2