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C3 elisa kit :: Complement C3 ELISA Kit

Scan QR to view Datasheet Catalog #    MBS135930 C3 elisa kit
Unit / Price
1 Kit  /  $435 +1 FREE 8GB USB
5 Kits  /  $1,805 +2 FREE 8GB USB
 
 Go to:   rightarrow  Product Names   rightarrow Product Info   rightarrow Accession #s   rightarrow Product Desc   rightarrow Diseases/Tissues/Pathways   rightarrow Applications   rightarrow References 
 Product Name   

Complement C3, ELISA Kit

★Popular Item★
 Also Known As   

Mouse Complement C3 ELISA kit

 Product Gene Name   

C3 elisa kit

[Similar Products]
 Research Use Only    For Research Use Only. Not for use in diagnostic procedures.
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  Sample Manual Insert    Download PDF Manual View PDF Manual
 Request for Current Manual Insert    Request Current Manual
 3D Structure    ModBase 3D Structure for P01027
 Host    Mouse
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 Specificity    This assay recognizes natural mouse C3. Pooled normal plasma from human, pig, rabbit, sheep, canine, and horse were assayed and no significant crossreactivity was observed. Pooled normal plasma from rat and rabbit resulted in significant color development.
 Form/Format    Complete kit
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 Preparation and Storage    Recommended Storage: 4 degree C
Minimum Shelf Life: 12 months from manufacture, see label for expiration date
Shipping Condition: Cold pack
 Product Note    Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
 Other Notes    Small volumes of C3 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
 Searchable Terms for C3 purchase    MBS135930 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Mouse Complement C3, ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing C3. The ELISA analytical biochemical technique of the MBS135930 kit is based on C3 antibody-C3 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect C3 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, C3. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
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 Product Categories/Family for C3 elisa kit    COMPLEMENT
Sample Manual Insert of MBS135930. Click to request current manual
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NCBI/Uniprot data below describe general gene information for C3. It may not necessarily be applicable to this product.
 NCBI GI #    126518317
 NCBI GeneID    12266
 NCBI Accession #    NP_033908.2 [Other Products]
 NCBI GenBank Nucleotide #    NM_009778.2 [Other Products]
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 UniProt Primary Accession #    P01027 [Other Products]
 UniProt Secondary Accession #    Q61370; Q80XP1 [Other Products]
 UniProt Related Accession #    P01027 [Other Products]
 Molecular Weight    60,952 Da [Similar Products]
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 NCBI Official Full Name    complement C3
 NCBI Official Synonym Full Names    complement component 3
 NCBI Official Symbol    C3 [Similar Products]
 NCBI Official Synonym Symbols   
ASP; Plp; HSE-MSF; AI255234
[Similar Products]
 NCBI Protein Information    complement C3; complement factor 3; complement component 3d; acylation stimulating protein
 UniProt Protein Name    Complement C3
 UniProt Synonym Protein Names   
HSE-MSFCleaved into the following 12 chains:Complement C3 beta chain; C3-beta-c; C3bc; Complement C3 alpha chain; C3a anaphylatoxin; Acylation stimulating protein; ASPAlternative name(s):C3adesArg
 Protein Family    Complement C3
 UniProt Gene Name    C3 [Similar Products]
 UniProt Synonym Gene Names    C3bc; ASP [Similar Products]
 UniProt Entry Name    CO3_MOUSE
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 NCBI Summary for C3    This gene encodes complement protein C3 which plays a central role in the classical, alternative and lectin activation pathways of the complement system. The encoded preproprotein undergoes a multi-step processing to generate various functional peptides. Mice deficient in the encoded protein fail to clear bacteria from the blood stream upon infection, display diminished airway hyperresponsiveness and lung eosinophilia upon allergen-induced pulmonary allergy, and develop severe lung injury after deposition of IgG immune complexes. Deficiency of the homolog of the encoded protein in humans was found to be associated with increased susceptibility to infections, age-related macular degeneration, and atypical hemolytic uremic syndrome. [provided by RefSeq, Mar 2015]
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 UniProt Comments for C3    C3: C3 plays a central role in the activation of the complement system. Its processing by C3 convertase is the central reaction in both classical and alternative complement pathways. After activation C3b can bind covalently, via its reactive thioester, to cell surface carbohydrates or immune aggregates. Defects in C3 are the cause of complement component 3 deficiency (C3D). A rare defect of the complement classical pathway. Patients develop recurrent, severe, pyogenic infections because of ineffective opsonization of pathogens. Some patients may also develop autoimmune disorders, such as arthralgia and vasculitic rashes, lupus-like syndrome and membranoproliferative glomerulonephritis. Genetic variation in C3 is associated with susceptibility to age-related macular degeneration type 9 (ARMD9). ARMD is a multifactorial eye disease and the most common cause of irreversible vision loss in the developed world. In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid that lie beneath the retinal pigment epithelium and within an elastin- containing structure known as Bruch membrane. Defects in C3 are a cause of susceptibility to hemolytic uremic syndrome atypical type 5 (AHUS5). An atypical form of hemolytic uremic syndrome. It is a complex genetic disease characterized by microangiopathic hemolytic anemia, thrombocytopenia, renal failure and absence of episodes of enterocolitis and diarrhea. In contrast to typical hemolytic uremic syndrome, atypical forms have a poorer prognosis, with higher death rates and frequent progression to end-stage renal disease. Susceptibility to the development of atypical hemolytic uremic syndrome can be conferred by mutations in various components of or regulatory factors in the complement cascade system. Other genes may play a role in modifying the phenotype. Increased levels of C3 and its cleavage product ASP, are associated with obesity, diabetes and coronary heart disease. Short-term endurance training reduces baseline ASP levels and subsequently fat storage.

Protein type: Secreted; Inhibitor; Secreted, signal peptide

Cellular Component: extracellular space; extracellular region

Molecular Function: protein binding; endopeptidase inhibitor activity; cofactor binding; lipid binding; C5L2 anaphylatoxin chemotactic receptor binding

Biological Process: positive regulation of developmental growth; immune system process; complement activation, alternative pathway; fatty acid metabolic process; complement activation; positive regulation of angiogenesis; positive regulation of activation of membrane attack complex; positive regulation of phagocytosis; positive regulation of G-protein coupled receptor protein signaling pathway; positive regulation of type IIa hypersensitivity; innate immune response; positive regulation of protein amino acid phosphorylation; lipid metabolic process; blood coagulation; inflammatory response; complement activation, classical pathway
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 Research Articles on C3    1. These results provide new insights into the role of systemic C3 in regulating contraction following intracellular bacterial infection and may help to develop vaccines that are more effective.
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 Precautions    All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
 Disclaimer    While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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Pathways associated with C3 elisa kitDiseases associated with C3 elisa kit
 Products by Pathway  Pathway Diagram
 Activation Of C3 And C5 Pathway antibodies  Activation Of C3 And C5 Pathway Diagram
 Adaptive Immune System Pathway antibodies  Adaptive Immune System Pathway Diagram
 Alternative Complement Activation Pathway antibodies  Alternative Complement Activation Pathway Diagram
 Chagas Disease (American Trypanosomiasis) Pathway antibodies  Chagas Disease (American Trypanosomiasis) Pathway Diagram
 Chagas Disease (American Trypanosomiasis) Pathway antibodies  Chagas Disease (American Trypanosomiasis) Pathway Diagram
 Class A/1 (Rhodopsin-like Receptors) Pathway antibodies  Class A/1 (Rhodopsin-like Receptors) Pathway Diagram
 Complement Activation, Classical Pathway antibodies  Complement Activation, Classical Pathway Diagram
 Complement And Coagulation Cascades Pathway antibodies  Complement And Coagulation Cascades Pathway Diagram
 Complement And Coagulation Cascades Pathway antibodies  Complement And Coagulation Cascades Pathway Diagram
 Complement And Coagulation Cascades Pathway antibodies  Complement And Coagulation Cascades Pathway Diagram
 Disease Name  Pubmed Publications
 Kidney Diseases Antibodies  >3670 publications with C3 and Kidney Diseases
 Cardiovascular Diseases Antibodies  >2414 publications with C3 and Cardiovascular Diseases
 Inflammation Antibodies  >1956 publications with C3 and Inflammation
 Proteinuria Antibodies  >1286 publications with C3 and Proteinuria
 Lung Diseases Antibodies  >1016 publications with C3 and Lung Diseases
 Pain Antibodies  >1009 publications with C3 and Pain
 Brain Diseases Antibodies  >953 publications with C3 and Brain Diseases
 Necrosis Antibodies  >934 publications with C3 and Necrosis
 Liver Diseases Antibodies  >930 publications with C3 and Liver Diseases
 Hemorrhage Antibodies  >777 publications with C3 and Hemorrhage
Organs/Tissues associated with C3 elisa kit
 Organ/Tissue Name  Pubmed Publications
 Blood Antibodies  >11910 publications with C3 and Blood
 Other Antibodies  >6655 publications with C3 and Other
 Kidney Antibodies  >3521 publications with C3 and Kidney
 Bone Antibodies  >2971 publications with C3 and Bone
 Skin Antibodies  >2276 publications with C3 and Skin
 Liver Antibodies  >1813 publications with C3 and Liver
 Muscle Antibodies  >1698 publications with C3 and Muscle
 Joint Antibodies  >1233 publications with C3 and Joint
 Lung Antibodies  >1103 publications with C3 and Lung
 Heart Antibodies  >1005 publications with C3 and Heart
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