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          • Primary Antibodies ›
          • Complement C5 Antibodies

          Invitrogen

          Complement C5 Polyclonal Antibody

          1 Published Figure
          1 Reference
          View all (28) Complement C5 antibodies

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          Cite Complement C5 Polyclonal Antibody

          Additional Information:
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          • Antibody Testing Data (1)
          • Published Figures (1)
          Complement C5 Antibody in Western Blot (WB)
          Group 53 Created with Sketch.
          Complement C5 Antibody in Western Blot (WB)
          Group 53 Created with Sketch.

          FIGURE: 1 / 2

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          Complement C5 Antibody (PA5-96933) in WB

          Western blot analysis of Complement C5 in mouse lung. Samples were incubated with Complement C5 Polyclonal antibody (Product # PA5-96933) using a dilution of 1:600, followed by HRP Goat Anti-Rabbit IgG (H+L) at a dilution of 1:10,000. Lysates/proteins: 25 µg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 90s. {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
          Published figure supplied by benchsci-logo
          PMID: {{$ctrl.currentElement.benchSciPubmedId}}
          View Product

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          Complement C5 Antibody in Western Blot (WB)
          Complement C5 Antibody in Immunocytochemistry (ICC/IF)

          Product Details

          PA5-96933

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          1:500-1:1,000
          -

          Immunocytochemistry (ICC/IF)

          -
          View 1 publication 1 publication

          ELISA (ELISA)

          1 µg/mL
          -
          Product Specifications

          Species Reactivity

          Human, Rat

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          Recombinant protein (or fragment)

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          0.42 mg/mL

          Amount

          42 µg

          Purification

          Affinity Chromatography

          Storage buffer

          PBS, pH 7.3, with 50% glycerol

          Contains

          0.05% ProClin 300

          Storage conditions

          -20°C, Avoid Freeze/Thaw Cycles

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          RRID

          AB_2808735

          Product Specific Information

          Positive Samples: U-937, Raji, Jurkat, Mouse heart, Rat liver

          Target Information

          C5 (Complement C5) is a Protein Coding gene. Diseases associated with C5 include Complement Component 5 Deficiency and Eculizumab, Poor Response To. Among its related pathways are GPCR downstream signalling and Acquired partial lipodystrophy / Barraquer-Simons syndrome. Gene Ontology (GO) annotations related to this gene include signaling receptor binding and endopeptidase inhibitor activity. An important paralog of this gene is C3. This gene encodes a component of the complement system, a part of the innate immune system that plays an important role in inflammation, host homeostasis, and host defense against pathogens. The encoded preproprotein is proteolytically processed to generate multiple protein products, including the C5 alpha chain, C5 beta chain, C5a anaphylatoxin and C5b. The C5 protein is comprised of the C5 alpha and beta chains, which are linked by a disulfide bridge. Cleavage of the alpha chain by a convertase enzyme results in the formation of the C5a anaphylatoxin, which possesses potent spasmogenic and chemotactic activity, and the C5b macromolecular cleavage product, a subunit of the membrane attack complex (MAC). Mutations in this gene cause complement component 5 deficiency, a disease characterized by recurrent bacterial infections. Alternative splicing results in multiple transcript variants.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

          Bioinformatics

          Protein Aliases: anaphylatoxin; anaphylatoxin C5; anaphylatoxin C5a analog; C3 and PZP-like alpha-2-macroglobulin domain-containing protein 4; C5a anaphylatoxin; Complement C5; Complement Component 5; CPAMD4; prepro-C5

          View more View less

          Gene Aliases: C5; C5a; C5b; C5D; CPAMD4; ECLZB; Hc; RGD1561905

          View more View less

          UniProt ID: (Human) P01031

          View more View less

          Entrez Gene ID: (Rat) 362119, (Human) 727

          View more View less

          Function(s)
          C5a anaphylatoxin chemotactic receptor binding G-protein coupled receptor binding endopeptidase inhibitor activity receptor binding protein binding chemokine activity receptor agonist activity protease inhibitor
          Process(es)
          in utero embryonic development leukocyte migration involved in inflammatory response cellular calcium ion homeostasis chemotaxis inflammatory response complement activation, alternative pathway complement activation, classical pathway positive regulation of vascular endothelial growth factor production negative regulation of norepinephrine secretion negative regulation of macrophage chemotaxis negative regulation of dopamine secretion glucose homeostasis positive regulation of angiogenesis positive regulation of chemotaxis positive regulation of chemokine secretion complement activation, lectin pathway immune system process regulation of immune system process complement activation signal transduction cell surface receptor signaling pathway G-protein coupled receptor signaling pathway cell migration leukocyte chemotaxis killing of cells of other organism positive regulation of chemokine production innate immune response regulation of chemotaxis cell chemotaxis complement activation, GZMK pathway
          It has to be done as per old AB suggested Products section.

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          If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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